CA is a Weekly Abstracting Journal

TW1

CA in Forsyth Library

TW2

• Chem Abstracts are located in the basement of Forsyth Library in the Index Area, which is located on the west side of the compact shelving.

Source of Abstracts, 1970(CAS monitors nearly 12,000 publications)

% of total No. of Sourcepapers in CA Journals 85% from 2000 75% from 1212 50% from 340 30% from 250 (core

journals)

25% from 50

TW5

Origin of Journal Abstracts, 1970 and 2005

CountryU.S. 27.4% 23.2%U.S.S.R. 23.6% 3.1%Japan 7.2% 11.2%Germany (E. & W.) 6.5% 6.9%U.K. 6.2% 4.2%France 4.1% 3.4%China — 14.1%All Others 25.0% 33.9%

72.6%

TW6

Language of Articles Abstracted 1966 and 2005

English 55% 83.2%Russian 21% 1.5%German 7% 1.3%French 5% 0.3%Japanese 3% 3.4%Chinese 0.5% 8.7%Other 8.5% 1.6%

TW7

One Volume at Forsyth…

TW8

… and its Indexes at Forsyth

TW12

Each Abstract is Classified Into One of Eighty Sections

TW13

Contents One Week…Biochemistry Sections1. History, education and documentation…...625672. General Biochemistry................................ 626233. Enzymes....................................................628834. Hormones and Related Subjects................630785. Radiation Biochemistry..............................633256. Biochemical Methods.................................634197. Plant Biochemistry......................................635678. Microbial Biochemistry...............................637479. Nonmammalian Biochemistry.....................6398110. Animal Nutrition..........................................6411911. Mammalian Biochemistry...........................6423512. Mammalian Pathological Biochemistry.......6452813. Immunochemistry.......................................6477114. Toxicology..................................................6485415. Pharmacodynamics....................................6491316. Fermentations............................................6533917. Foods.........................................................6541918. Plant-Growth Regulators............................6557919. Pesticides...................................................6571220. Fertilizers, Soils, and Plant Nutrition...........65897

TW14

Contents One Week…Organic Chemistry Sections21. General Organic Chemistry..............................…..6601322. Physical Organic Chemistry..............................….6602623. Aliphatic Compounds................................………..6626224. Alicyclic Compounds ............................................6043425. Noncondensed Aromatic Compounds..............…..6649926. Condensed Aromatic Compounds.........................6667027. HeterocycIic Compounds (One Hetero Atom)…... 6671428. Heterocyclic Compounds (More Than One Hetero

Atom..............................................................….... 6684929. Organometallic and Organometalloidal

Compounds ...............................................................................67007

30. Terpenoids ..........................................………....…6711731. Alkaloids ............................................................…6714932. Steroids ..........................................................……6716933. Carbohydrates........................................................6721634. Synthesis of Amino Acids, Peptides, and

Proteins..................................................................67230

TW15

…and Contents the next Week…• …include 12 sections of Macromolecular

Chemistry…Macromolecular Chemistry Sections35. Synthetic High Polymers.......…………………5590036. Plastics Manufacture and Processing………..5611037. Plastics Fabrication and Uses………………...5635538. Elastomers, Including Natural Rubber……….5643639. Textiles……………………………………….….5651940. Dyes, Fluorescent Whitening Agents, and

Photosensitizers…………………………………5666441. Leather and Related Materials………………..5672142. Coatings, Inks, and Related Products……….5674043. Cellulose, Lignin, Paper, and Other Wood Products

…………………………………………….…..…..5682444. Industrial Carbohydrates………………………5694445. Fats and Waxes………………………….……..5697946. Surface-Active Agents and Detergents………57000

TW16

…and Contents the next Week……18 sections are concerned with Applied Chemistry and

Chemical Engineering…Applied Chemistry and Chemical Engineering Sections47. Apparatus and Plant Equipment…………………………………5702948. Unit Operations and Processes………………………………….5707849. Industrial Inorganic Chemicals……………………………………5724550. Propellants and Explosives…………………………………. …...5734451. Petroleum, Petroleum Derivatives, and Related Products…….5736752. Coal and Coal Derivatives………………………………………..5751953. Mineralogical and Geological Chemistry………………………..5755654. Extractive Metallurgy………………………………………………5788555. Ferrous Metals and Alloys………………………………………...5797656. Nonferrous Metals and Alloys…………………………………….5822757. Ceramics…………………..………………………………….…….5854358. Cement and Concrete Products………………………………….5868559. Air Pollution and Industrial Hygiene……………………………..5879560. Sewage and Wastes………………………………………………5884061. Water………………………………………………………………..5889162. Essential Oils and Cosmetics…………………………………….5897063. Pharmaceuticals……………………………………………………5899664. Pharmaceutical Analysis…………………………………………..59100

TW17

…and Contents the next Week……and finally 16 sections are concerned with Physical and

Analytical ChemistryPhysical and Analytical Chemistry Sections65. General Physical Chemistry…………………………………….5914366. Surface Chemistry and Colloids……………………………..5944067. Catalysis and Reaction Kinetics……………………………..5960068. Phase Equilibriums, Chemical Equilibriums, and Solutions…5969169. Thermodynamics, Thermochemistry, and Thermal Properties……………………………………………………………..5989270. Crystallization and Crystal Structure……………………..……5997171. Electric Phenomena……………………………………..………6021272. Magnetic Phenomena…………………………………………...6064073. Spectra by Absorption, Emission, Reflection,or Magnetic

Resonance, and Other Optical Properties…………………….6077274. Radiation Chemistry, Photochemistry, and Photographic

Processes………………………………………………..6127275. Nuclear Phenomena………………………………………..6144576. Nuclear Technology……………………………………………..6185977. Electrochemistry………………………………………………….6208578. Inorganic Chemicals and Reactions…………………………...6230579. Inorganic Analytical Chemistry…………………………………6240380. Organic Analytical Chemistry…………………………………...62532

TW18

TW19

Abstracts

• Often appear within a month of the date of publication of articles from major journals

• May appear anywhere from the date of publication of an article to one year later

• With the advent of online publishing, they may appear before the journal is printed (JBC PIP)…

• …and can disappear before publication if a paper is withdrawn

TW19b

A Typical Abstract: Title

TW20

55913s Optimal control of polymerization reactors. Hicks, James; Mohan, Amar; Ray, Willis Harmon (Dep. Chem. Eng., Univ. Waterloo, Waterloo, Ont.). Can. J. Chem. Eng. 1969, 47(6), 590-7 (Eng). The optimal control policy for continuous stirred tank polymn. reactors and the optimal control program for batch polymn. reactors are discussed. The first problem concerns detg. the temp. and initiator control policy which brings the reactor to the desired steady state while minimizing some objective functional (e.g. start-up time, cost of control action, etc.). The second problem is concerned with finding the temp. and initiator program so that the product from the batch reactor has the best possible mol. wt. distribution. Both free-radical polymn. and linear condensation polymn. examples are considered with mol. wt. distribution moments being used to characterize the polymer. Kinetic parameters typical of styrene are used for the free radical case, and realistic parameters are chosen for the condensation examples. Some of the potential gains possible through supervisory computer control of polymn. reactors are demonstrated. RCHC

A Typical Abstract: Authors and Institution Affiliation

55913s Optimal control of polymerization reactors. Hicks, James; Mohan, Amar; Ray, Willis Harmon (Dep. Chem. Eng., Univ. Waterloo, Waterloo, Ont.). Can. J. Chem. Eng. 1969, 47(6), 590-7 (Eng). The optimal control policy for continuous stirred tank polymn. reactors and the optimal control program for batch polymn. reactors are discussed. The first problem concerns detg. the temp. and initiator control policy which brings the reactor to the desired steady state while minimizing some objective functional (e.g. start-up time, cost of control action, etc.). The second problem is concerned with finding the temp. and initiator program so that the product from the batch reactor has the best possible mol. wt. distribution. Both free-radical polymn. and linear condensation polymn. examples are considered with mol. wt. distribution moments being used to characterize the polymer. Kinetic parameters typical of styrene are used for the free radical case, and realistic parameters are chosen for the condensation examples. Some of the potential gains possible through supervisory computer control of polymn. reactors are demonstrated. RCHC

TW21

A Typical Abstract: Complete Citation

TW22

55913s Optimal control of polymerization reactors. Hicks, James; Mohan, Amar; Ray, Willis Harmon (Dep. Chem. Eng., Univ. Waterloo, Waterloo, Ont.). Can. J. Chem. Eng. 1969, 47(6), 590-7 (Eng). The optimal control policy for continuous stirred tank polymn. reactors and the optimal control program for batch polymn. reactors are discussed. The first problem concerns detg. the temp. and initiator control policy which brings the reactor to the desired steady state while minimizing some objective functional (e.g. start-up time, cost of control action, etc.). The second problem is concerned with finding the temp. and initiator program so that the product from the batch reactor has the best possible mol. wt. distribution. Both free-radical polymn. and linear condensation polymn. examples are considered with mol. wt. distribution moments being used to characterize the polymer. Kinetic parameters typical of styrene are used for the free radical case, and realistic parameters are chosen for the condensation examples. Some of the potential gains possible through supervisory computer control of polymn. reactors are demonstrated. RCHC

A Typical Abstract: Language

TW23

55913s Optimal control of polymerization reactors. Hicks, James; Mohan, Amar; Ray, Willis Harmon (Dep. Chem. Eng., Univ. Waterloo, Waterloo, Ont.). Can. J. Chem. Eng. 1969, 47(6), 590-7 (Eng). The optimal control policy for continuous stirred tank polymn. reactors and the optimal control program for batch polymn. reactors are discussed. The first problem concerns detg. the temp. and initiator control policy which brings the reactor to the desired steady state while minimizing some objective functional (e.g. start-up time, cost of control action, etc.). The second problem is concerned with finding the temp. and initiator program so that the product from the batch reactor has the best possible mol. wt. distribution. Both free-radical polymn. and linear condensation polymn. examples are considered with mol. wt. distribution moments being used to characterize the polymer. Kinetic parameters typical of styrene are used for the free radical case, and realistic parameters are chosen for the condensation examples. Some of the potential gains possible through supervisory computer control of polymn. reactors are demonstrated. RCHC

A Typical Abstract: Abstracter

TW24

55913s Optimal control of polymerization reactors. Hicks, James; Mohan, Amar; Ray, Willis Harmon (Dep. Chem. Eng., Univ. Waterloo, Waterloo, Ont.). Can. J. Chem. Eng. 1969, 47(6), 590-7 (Eng). The optimal control policy for continuous stirred tank polymn. reactors and the optimal control program for batch polymn. reactors are discussed. The first problem concerns detg. the temp. and initiator control policy which brings the reactor to the desired steady state while minimizing some objective functional (e.g. start-up time, cost of control action, etc.). The second problem is concerned with finding the temp. and initiator program so that the product from the batch reactor has the best possible mol. wt. distribution. Both free-radical polymn. and linear condensation polymn. examples are considered with mol. wt. distribution moments being used to characterize the polymer. Kinetic parameters typical of styrene are used for the free radical case, and realistic parameters are chosen for the condensation examples. Some of the potential gains possible through supervisory computer control of polymn. reactors are demonstrated. RCHC

A Typical Abstract: ID tag

TW25

55913s Optimal control of polymerization reactors. Hicks, James; Mohan, Amar; Ray, Willis Harmon (Dep. Chem. Eng., Univ. Waterloo, Waterloo, Ont.). Can. J. Chem. Eng. 1969, 47(6), 590-7 (Eng). The optimal control policy for continuous stirred tank polymn. reactors and the optimal control program for batch polymn. reactors are discussed. The first problem concerns detg. the temp. and initiator control policy which brings the reactor to the desired steady state while minimizing some objective functional (e.g. start-up time, cost of control action, etc.). The second problem is concerned with finding the temp. and initiator program so that the product from the batch reactor has the best possible mol. wt. distribution. Both free-radical polymn. and linear condensation polymn. examples are considered with mol. wt. distribution moments being used to characterize the polymer. Kinetic parameters typical of styrene are used for the free radical case, and realistic parameters are chosen for the condensation examples. Some of the potential gains possible through supervisory computer control of polymn. reactors are demonstrated. RCHC

CAS Numbers First Appeared in 1972

670d Osmotic pressure and macromolecular conformation. Charmasson, Rene (Lab. Phys. Liq., Fac. Sci., Marseilles, Fr.). C.R. Acad. Sci. Ser. C 1971. 272(3). 256-7 (Fr). The thermodynamics of the

N O

CH2CH

nI

TW31

Van’t Hoff law of OSMOTIC PRESSURE variation with concn. was studied for dil. solns. of sucrose [57-50-1], dextran, and poly(vinylpyrrolidone) (I) [9003-39-8]. Due to solvent constraints, the solutes were changed from their preferential, unperturbed state causing a pressure shock which modified the mol. CONFIGURATION.

Indicative Abstracts

TW32

Abstracts Give Little Information…

TW34

105898x Preparation and synthetic utility of -vinylperfluoro-alkanecarboxylates. Kim, Yung K.; Pierce, Ogden R. (Fluorine Res. Lab., Dow Corning Corp., Midland, Mich.). J. Org. Chem. 1969, 34(3), 602-5 (Eng). The addn. of ethylene to ethyl -bromoperfluoroalkanecarboxylates under free-radical conditions gave the desired 1: 1 adduct, BrCH2CH2 (CF2CF2)nCOO2Et, in good yield along with the 1 :2 adduct, Br(CH2CH2)2(CF2CF2),CO2Et, and a little of the higher telomers. Treatment of the I : 1 adduct with NaOEt resulted in the formation of Et -(vinyl)perfluoroalkanecarboxylates in high yield. Et 3-(vinyl)perfluoro-propionate was converted into 3-(vinyl)perfluoropropionitrile (I) via the corresponding amide. The synthetic approach leading to a fluorosilicone-triazine polymer, -[-SiMe(CH3)(CF3CH2CH2)CH2CH2CF2CF2 (CF3C3N3)-CF2CF2CH2CH2 (CF3CH2CH2)MeSiO-]-, (where CF3C3N3 is 6-trifluoromethyltriazine-2,4-diol), by utilization of I is described.

…Papers Give Much More

TW35

…Papers Give Much More

TW36

Each Weekly Issue Contains:

• Author Index• Numerical Patent Index• Patent Concordance• Keyword Index

TW37

Author Index

TW37b

Author Index Allowing Explication

Van Eck J 58833tVan Geldrop L M 60347fVanheertum J J 59406tVan Hemert R L 59983dVan Huyssteen J J 60671gVanin V S 60050dVan Itterbeek A 57510y

TW37c

TW38

Keyword Subject Index

TW43

45

Subject IndexTW46

Subject Index

Abetinol. See Podocarpa-7,13-dien-15-ol, 13- isopropyl-Abietyl alcohol (abietinol). See Podocarpa- 7,13-dien-15-ol, 13-

isopropyl-_____, dehydro-. See Podocarpa-7,11,13-trien-15-ol, 13-

isopropyl-_____, tetrahydro-. See Podocarpan-15-ol, 13-isopropyl-Abietylamine, dehydro-

acetate, quartz flotation by, adsorption and contact angles in relation to, 66:5968qreaction products with dialkyl and monoalkyl phosphates, gelation of, 66:P 38490kreaction product with ethylene oxide phosphoric acid, as lubricating oil for metal

TW46b

Subject Index

JAN-JUN 1967—SUBJECT INDEX Ferroceno[1,2]cyclohex-1-ene-3,6-dione

___, 3-phenyl-, 66:55568jFerrocenecarbonyl Chloride

poIymers, 66:11198jFerrocenecarboxaldehyde 66:85846r

chromatog. of 66:121854cpolarography of, in aq. ethyl alc., 66:78889u

___,1’,2-dimethyI-nuclear magnetic resonance of, 66:104562p

___,1' ,3-dimethylnuclear magnetic resonance of, 66:104562p

TW47

TW48

TW49

TW50

Chemical Abstracts – Vol. 65

spectrum of, 65: 9943fStrontium nickel antimonate (V)

NiSr3Sb2O4, crystal field theory and spectrum of, 65: 9851b

Strontium nickel molybdate (VI)NiSr2MO6, crystal and magnetic structure and elec. and magnetic properties of, 65:4822c

Strontium nickel niobate (V)NiSr3Nb2O6, crystal field theory and spectrum of, 65:9851b

TW51

TW52

TW53

TW54

TW55

TW56

Hill Indexing System(Modified) for

Compounds Containing Carbon

CARBON, HYDROGEN, THEN ALPHABETICALLY

TW57

Formulas are Arranged AlphabeticallyExample I

Al6Ca5O14

C2H5AlBr2

TW58a

Formulas are Arranged AlphabeticallyExample II

CCl4CH

CHCl3CO

C2Ca

TW58d

TW59C2H2I2

Ethylene, 1,2-diiodo-, 63:5480f C2H2MgO6

See Magnesium carbonateC2H2MnO4

Manganese formate, 63:136fdihydrate, 63:6406b, 7750e

C2H2NAmidogen, vinylidene-, 63:15753bMethyl, cyano-, 63:8174a

C2H2N2

Acetonitrile, imino-, 63:1331dMethylene, aminocyano-, 63:1331d

C2H2N2OFurazan, 63:2540f, 4120c, 9253c

TW60C2H2I2

Ethylene, 1,2-diiodo-, 63:5480f C2H2MgO6

See Mangnesium carbonateC2H2MnO4

Manganese formate, 63:136fdihydrate, 63:6406b, 7750e

C2H2NAmidogen, vinylidene-, 63:15753bMethyl, cyano-, 63:8174a

C2H2N2

Acetonitrile, imino-, 63:1331dMethylene, aminocyano-, 63:1331d

C2H2N2OFurazan, 63:2540f, 4120c, 9253c

TW62C2H2O4

See Oxalic acidC2H2O4Rh

Rhodium formate, 63:12668dhydrate, 63:13083c

C2H2O4Sn

Tin formate 63:2535ce, 9426d, P 10130aC2H2O4Zn

Zinc formate, 63:P 3074aC2H2O4U

Uranyl formate, 63:16761dC2H2T2

Ethylene-1,2-t2, 63:P 15714d

70

10-Digit CAS Registry Numbers Coming in Mid-January 2008

TW71

Probably, 54 arises from fluoride ion trapping either the initial carbonium ion or one of the other intermediates that usually leads to 50 or 53.

C2H5C

NF2CCH2CH3

NF2

NF

C2H5C N

F

CCH2CH3

NF2

NF2

12

53

+ C2H5C N

F

CCH2CH3NF2

F

54

Both the 4-chloro- and 4-methoxylphenylfluorimines (13 and 14, respectively) gave small amounts of the

TW72

Registry Numbers in Article

14, 20122-80-9; 15, 20122-81-0; 1626, 19955-15-8; 27, 20122-81-3; 2829, 20122-85-5; 30, 20122-87-6; 3132, 20122-89-8; 33, 20122-90-1; 3437a, 20122-92-3; 37b, 20122-93-4 3839, 20122-95-6; 45, 20122-96-7; 4647, 20116-42-1; 53, 20116-43-2; 5457, 20116-45-4; 58, 20116-46-5; 5960, 20116-48-7; 66, 20116-49-8 67

TW73

20116-40-9 2,3-Butanediamine, 2-chloro-N,N,N’,N’-tetrafluoro- C4H7ClF4N2

20116-41-0 Benzimidoyl fluoride, N-[1,1-bis(difluoroamino)ethyl]-p-chloro- C9H7ClF5N3

20116-42-1 1,1-Ethanediamine, 1-[[1-difluoroamino)-1-fluoroethyl]azo]-N,N,N’,N’-tetrafluoro- C4H6F7N5

20116-43-2 Benzimidoyl fluoride, N-[1,1-bis(difluoroamino)propyl]- C10H10F5N3

20116-44-3 Benzimidoyl fluoride, N-[1-(difluoroamino)-1-fluoropropyl]- C10H10F5N3

20116-45-4

Registry Numbers Index

TW74 Benzimidoyl chloride——, N-benzoyl- [25250-38-8]

promoters, for sodium hydride and sodium methoxide catalyts for polymn. of hexahydroazepinone, 81906r

——, N-(o-cyanophenyl)- [15437-26-0], 80908f——, N-(2,6-dichlorophenyl)- [23695-48-9], 80908f——, N-o-tolyl- [19053-49-7], 80908fBenzimidoyl fluoride——, N-[1,1-bis(difluoroamino)ethyl]-p-chloro- [20116-41-0],

70208p——, N-[1,1-bis(difluoroamino)propyl]-

[20116-43-2], 70208p——, N-[1,1-(difluoroamino)-1-fluoropropyl]

[20116-44-3], 70208pBenzimidoyl isothiocyanate——, p-chloro-N-(p-chloorophenyl)-

[23938-13-8], 101761v

TW75Convallariakeiskei and majalis and transcoucosica,

chimononthine in leaves of, 98960bmajalis

glycosides of, detn. of photocolorimetry,24756t

photosynthesis by, ecological-physiol.features of, 12057a

Convallatoxin [508-75-8]biol. activity of, 20612vin Convallaria, 89860bheart response to, hawthorn ext. effect on,

20667sMetabolism of, in intestines, 48170y

TW76

508-71-4 8α, 10ß-Ros-15-en-19-oic acis, 10-hydroxy-7-oxo-, γ-lactone C20H28O3

508-75-8 Convallatoxin C29H42O10

508-76-9 Corchoroside A C29H42O10

508-77-0 Cymarin C30H44O9

509-14-8 Methane, tetranitro- CN4O8

509-18-2 Delsoline C25H41NO7

509-36-4 ß-Colubrine C22H42N2O3

TW77

C29H42O9

Corchoroside [508-76-9], 73979bCorchoroside A [508-76-9], P 6530kHelveticoside [630-64-8], P 6530k, 48170y

C29H42O9

Atisane-17,18-dioic acid, 15α-carboxy-13,16-epoxy-14,15-dihydroxy-13-isopropyl-trimethyl ester, 14-acetate, (-)-[25452-10-2], 22210mConvallatoxin [508-75-8], 20612v, 20667s, 48170y, 98960b

Molecules With More Than One Name

OHH2N

p-aminophenolp-hydroxyaniline

TW95

TW96 C6H7NO

Hydroxylamine, N-phenyl-, 86425k, 108349tKetone, methyl pyrrol-2-yl, 99040f

6-Oxabicyclo(3,1,0)hexane-1-carbonitrile, 64123hPhenol, m-amino-, 14896s, 25432p, P44643z,

78769k, P82914w, 84760s, 94047d, 99815n,102844d, 107890a

compd. with boron chloride (BCl3) (3:1), 2831d

——, o-amino-, 9925w, 14896s, 62249e, 62695x,compd. with boron chloride (BCl3) (3:1), 2831d

polymer with (propylphosphinidene)dimethanol,117415p

——, p-amino-, See Subject Indexcompd. with boron chloride (BCl3) (3:1), 2831d

TW97

Aniline, N-(2-ethyl-2,3-butadienyl)-

——, 2-(hexadecyloxy)-5-(methylsulfonylP 109643w

——, hexahydro-, See Cyclohexylamine——, p-(hexylthio)-, 67:43495r——, ar-hydroxy-, See Phenol, amino-

——, N-hydroxy-, See Hydroxylamine, N——, N-(2-hydroxyethyl)-. See Ethanol,

lino-——, 4,4’-imidocarbonylbis N,N-dimethy

TW98

Phenol, p-allyl-

metabolism of, by liver, diethylaminoethyl diphenylpropylacetic acid effect on, 67:62695x

polymer with (propylphosphinidene)dimethanol, prepn. and properties of, 67: 117415p

reaction of, with 2,2-dihydroxy-1,3-indandione, mechanism of, 67:107890a

——, p-amino-as p-acetamidophenol and phenacetin

metabolit in urine, primary substance detn. in

TW100

Aniline, N-hexadecyl

——, N-hexadienyl-, See Hexadienylamine, N-phenyl-——, hexahydro-, See Cyclohexylamine——, N-hexatrienyl-, See Hexatrienylamine, N-phenyl-——, N-hexyl-, See Hexylamine, N-phenyl-——, ar-hydroxy-, See Phenol, amino-——, N-hydroxy-, See Hydroxylamine, N-phenyl-——, N-(2-hydroxyethyl)-, See Ethanol, 2-anili-

Functions by Class Namein Descending Order of PrecedenceisocyanidesaldehydesketonesthionesalcoholsphenolsthiolshydroperoxidesGroup V oxides, sulfides, selenides, tellurides, imidesaminesphosphinesphosphoranesremaining trivalent Group V hydrides

TW102

Ring System Usage

Number of rings = 2Size of rings = 4,5Elemental analysis of rings = C3N-C4O

NO

CO2H

TWnew

2-RING SYSTEMS

4,5CNOP-C2NOP

2,7-Dioxa-5-aza-1-phosphabicyclo[3.2.0]heptaneC2B2-C2B3

2,3,5,6-Tetraborabicyclo[2.1.1]hexane... C3N-C4N

1-Azabicyclo[3.2.0]heptane C3N-C4O

2-Oxa-7-azabicyclo[3.2.0]heptane3-Oxa-6-azabicyclo[3.2.0]heptane

TWnew

Indexes in Volumes

1st-4th Author, Subject5th Author, Subject, Numerical Patent, Formula6th Author, Subject (incl. Ring), Numerical Patent,

Formula7th Author, Subject (incl. Ring), Numerical Patent,

Formula, Patent Concordance8th Author, Subject, Numerical Patent, Formula-Ring,

Patent Concordance, Registry Handbook, Index Guide9th Author, Subject, Numerical Patent, Formula-Ring,

Patent Concordance, Chemical Substance Index, Registry Handbook, Index Guide and Index Guide Supplements

TW103

Indices

1907 Author Index1907 Subject Index1916 Index of Ring

Systems1920 Formula Index1935 Numerical Patent Index1963 Patent Concordance1968 Index Guide

General Subject Index Chemical Substance Index

Combined 1981 – – Patent

Index

TW

Collective Indices10 Year Collective 5 Year Collective (1907-1956) (1957-1976)

1st 1907-1916 4v. 6th 1957-1961 15v.2nd 1917-1926 5v. 7th 1962-1966 24v.3rd1927-1936 5v. 8th 1967-1971 34v.4th 1937-1946 6v. 9th 1972-1976 62±1v.5th 1947-1956 14v.

14th 1997-2001 431,642 pages (9th had 95,882 pages)

The week of July 30, 2007 established a new record of 24,623 records added

TW104