28338-70-7 Usage
Description
(9S,14S)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene is a complex organic compound characterized by its cyclopenta[a]phenanthrene structure. It features both methyl and heptan-2-yl groups, and is classified as a dodecahydro compound due to the presence of 12 hydrogen atoms. This unique structure and properties make it a promising candidate for various applications in the pharmaceutical and industrial sectors, and it may also be utilized in the synthesis of other organic compounds. Due to its complex structure and potential reactivity, it is important to handle and use this chemical with caution.
Uses
Used in Pharmaceutical Applications:
(9S,14S)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure allows it to interact with biological targets, making it a candidate for the development of new drugs and therapies.
Used in Industrial Applications:
In the industrial sector, (9S,14S)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene is used as an intermediate in the synthesis of other organic compounds. Its complex structure and reactivity make it a valuable component in the production of various chemical products.
Used in Chemical Synthesis:
(9S,14S)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene is used as a key component in the synthesis of other organic compounds. Its unique structure and properties enable it to serve as a building block for the creation of new molecules with specific functions and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 28338-70-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,3 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28338-70:
(7*2)+(6*8)+(5*3)+(4*3)+(3*8)+(2*7)+(1*0)=127
127 % 10 = 7
So 28338-70-7 is a valid CAS Registry Number.
InChI:InChI=1/C27H46/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h12-13,19-25H,6-11,14-18H2,1-5H3/t20-,21?,22?,23?,24+,25+,26?,27?/m1/s1
28338-70-7Relevant articles and documents
Stereochemistry and Regiochemistry of Electron Impact, Photolytically, and Thermally Induced Eliminations from 5α-Cholestanyl Acetates
Valente, C.,Eadon, G.
, p. 44 - 51 (2007/10/02)
Deuterium-labeled compounds were used to define the sterochemistry and regiochemistry of the electron impact induced eliminations of acetic acid from 5α-cholestanyl 3α-acetate, 4α-acetate, and 6α-acetate.Comparison of the electron impact induced eliminations to the pyrolysis and to the photolysis of the corresponding phenylacetates confirmed that the mass spectral elimination was a stepwise process proceeding through the stable chair conformation of the steroid's cyclohexyl ring.The equatorially oriented 4α- and 6α-acetates fragmented with predominant loss of asecondary trans-equatorial hydrogen, rather than the tertiary cis-axial hydrogen, despite the a priori greater migratory aptitude of tertiary hydrogens.The electron impact induced fragmentation of the 3α-acetate occured with predominant loss of a C-4 hydrogen; in contrast, the photolysis of the corresponding 3α-phenylacetate results in loss of a C-2 hydrogen.This results can be attributed to the reversibility of the photolytically induced hydrogen-abstraction step.
