10062-39-2 Usage
Description
3-Aza-A-homocholest-4a-en-4-one is a member of the class of caprolactams that is derived from the Beckmann rearrangement of the oxime derivative of cholest-4-en-3-one. It is a chemical compound with a unique structure that has potential applications in various fields due to its specific properties.
Uses
Used in Pharmaceutical Industry:
3-Aza-A-homocholest-4a-en-4-one is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Research:
In the field of chemical research, 3-Aza-A-homocholest-4a-en-4-one serves as a valuable compound for studying the properties and reactions of caprolactams and their derivatives. This can lead to a better understanding of their potential applications and the development of new chemical processes or products.
Used in Material Science:
3-Aza-A-homocholest-4a-en-4-one may also find applications in material science, where its unique structure could be utilized to create new materials with specific properties. These materials could have potential uses in various industries, such as electronics, aerospace, or automotive.
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
10062-39-2Relevant articles and documents
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Billett,E.H. et al.
, p. 1661 - 1668 (1973)
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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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