57759-45-2 Usage
Uses
Used in Pharmaceutical Applications:
(3S,8S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol is used as a potential pharmaceutical agent for its possible involvement in biological processes. Its complex and highly symmetrical structure suggests that it may have unique properties that could be harnessed for medicinal purposes.
Used in Medical Applications:
In the medical field, (3S,8S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol may be utilized for its potential applications in treating various conditions. Its chiral centers and complex structure could provide novel mechanisms of action for therapeutic interventions.
Used in Research Applications:
(3S,8S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol is used as a subject of research to further explore its properties, potential uses, and mechanisms of action. Understanding its interactions with biological systems could lead to the development of new drugs or therapies.
Used in Chemical Synthesis:
In the field of chemical synthesis, (3S,8S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol may serve as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structure and chiral centers could be valuable in creating novel molecules with specific properties.
Check Digit Verification of cas no
The CAS Registry Mumber 57759-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,5 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 57759-45:
(7*5)+(6*7)+(5*7)+(4*5)+(3*9)+(2*4)+(1*5)=172
172 % 10 = 2
So 57759-45-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H46O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h9,18-19,21-25,28H,6-8,10-17H2,1-5H3/t19-,21+,22+,23-,24-,25+,26+,27-/m1/s1
57759-45-2Relevant academic research and scientific papers
STEREOCONTROLLED SYNTHESIS OF STEROID SIDE CHAIN; STEREOSELECTIVE SYNTHESES OF CHOLESTEROL AND 25-HYDROXYCHOLESTEROL
Ohmori, Masayuki,Yamada, Sachiko,Takayama, Hiroaki
, p. 4709 - 4712 (2007/10/02)
Novel stereoselective method to introduce side chain onto 17-oxosteroids has been deviced, and using the method cholesterol and 25-hydroxycholesterol are synthesized.
β-(Trimethylsilyl)ethoxymethyl chloride. A new reagent for the protection of the hydroxyl group
Lipshutz, Bruce H.,Pegram, Joseph J.
, p. 3343 - 3346 (2007/10/02)
Reactions of β-(trimethylsilyl)ethoxymethyl chloride with alcohols afford the corresponding ethers in high yield. Deprotection using n-Bu4NF in THF or HMPA cleanly regenerates the hydroxyl function.
Synthesis of steroids
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, (2008/06/13)
In the synthesis of sterols wherein methoxyethoxymethyl groups in an ether linkage are attached to the nucleus of the sterol to protect the sterol nucleus during other steps of the synthesis and the sterols are thereafter treated to remove the methoxyethoxymethyl groups and set free the hydroxyl groups, the improvement in which the sterols being treated with zinc bromide are held in a methylene chloride solution containing a small amount of an aliphatic alcohol having from 1 to 6 carbon atoms.
