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10062-39-2

10062-39-2

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  • Cyclopenta[5,6]naphth[1,2-d]azepin-2(3H)-one,8-[(1R)-1,5-dimethylhexyl]-4,5,5a,5b,6,7,7a,8,9,10,10a,10b,11,12-tetradecahydro-5a,7a-dimethyl-,(5aR,5bS,7aR,8R,10aS,10bS)-

    Cas No: 10062-39-2

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  • Cyclopenta[5,6]naphth[1,2-d]azepin-2(3H)-one,8-[(1R)-1,5-dimethylhexyl]-4,5,5a,5b,6,7,7a,8,9,10,10a,10b,11,12-tetradecahydro-5a,7a-dimethyl-,(5aR,5bS,7aR,8R,10aS,10bS)-

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  • Cyclopenta[5,6]naphth[1,2-d]azepin-2(3H)-one,8-[(1R)-1,5-dimethylhexyl]-4,5,5a,5b,6,7,7a,8,9,10,10a,10b,11,12-tetradecahydro-5a,7a-dimethyl-,(5aR,5bS,7aR,8R,10aS,10bS)- cas 10062-39-2

    Cas No: 10062-39-2

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  • Cyclopenta[5,6]naphth[1,2-d]azepin-2(3H)-one,8-[(1R)-1,5-dimethylhexyl]-4,5,5a,5b,6,7,7a,8,9,10,10a,10b,11,12-tetradecahydro-5a,7a-dimethyl-,(5aR,5bS,7aR,8R,10aS,10bS)-

    Cas No: 10062-39-2

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10062-39-2 Usage

Definition

ChEBI: A member of the class of caprolactams resulting from the Beckmann rearrangement of the oxime derivative of cholest-4-en-3-one.

Check Digit Verification of cas no

The CAS Registry Mumber 10062-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,6 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10062-39:
(7*1)+(6*0)+(5*0)+(4*6)+(3*2)+(2*3)+(1*9)=52
52 % 10 = 2
So 10062-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H45NO/c1-18(2)7-6-8-19(3)22-11-12-23-21-10-9-20-17-25(29)28-16-15-26(20,4)24(21)13-14-27(22,23)5/h17-19,21-24H,6-16H2,1-5H3,(H,28,29)/t19-,21+,22-,23+,24+,26+,27-/m1/s1

10062-39-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-aza-A-homocholest-4a-en-4-one

1.2 Other means of identification

Product number -
Other names 3-Aza-A-homo-4a-cholesten-4-on

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10062-39-2 SDS

10062-39-2Relevant articles and documents

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Billett,E.H. et al.

, p. 1661 - 1668 (1973)

-

PHOTO-INDUCED MOLECULAR TRANSFORMATIONS.PART 87. REGIOSPECIFIC PHOTO-BECKMANN REARRANGEMENT OF STEROIDAL α,β-UNSATURATED KETONE OXIMES: SYNTHESIS OF SOME STEROIDAL ENAMINO LACTAMS

Suginome, Hiroshi,Kaji, Makoto,Yamada, Shinji

, p. 321 - 326 (2007/10/02)

While it is well known that the Beckmann rearrangement of steroidal cyclic α,β-unsaturated ketone oximes lead to the exclusive formation of enone-type lactams regardless of the initial geometry of their hydroxyimino group, the photolysis of three isomeric cholestenone oximes, (E)- and (Z)-cholest-4-en-3-one oximes, (E)-2,2-dimethylcholest-4-en-3-one oxime, and (E)-cholest-5-en-7-one oxime in protic solvents has shown that in each case an enamine-type lactam is the sole product (yield/=33 percent), no enone-type lactam being formed.This regiospecific photo-rearrangement may be of value for the preparation of these enamine-type lactams which cannot be achieved by the Beckmann rearrangement.

Ring expansion of cyclic ketones: The reliable determination of migration ratios for 3-keto steroids by 13C nuclear magnetic resonance and the general implications thereof

Dave,Stothers,Warnhoff

, p. 1557 - 1568 (2007/10/09)

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