Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C27H45Cl |
| Molecular Weight | 405.099 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]1(CC[C@@]2([H])[C@]3([H])CC=C4C[C@@H](Cl)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C
InChI
InChIKey=OTVRYZXVVMZHHW-DPAQBDIFSA-N
InChI=1S/C27H45Cl/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/h9,18-19,21-25H,6-8,10-17H2,1-5H3/t19-,21+,22+,23-,24+,25+,26+,27-/m1/s1
| Molecular Formula | C27H45Cl |
| Molecular Weight | 405.099 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 8 / 8 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Theoretical mechanism of the formation of cholesteryl chloride from cholesterol and thionyl chloride. | 2005 Mar |
|
| Validation of a one-step extraction/methylation method for determination of fatty acids and cholesterol in marine tissues. | 2006 Feb 3 |
|
| Cholesterol hemisuccinate: a selective inhibitor of family X DNA polymerases. | 2007 Mar 9 |
|
| Inhibitory effects of cholesterol derivatives on DNA polymerase and topoisomerase activities, and human cancer cell growth. | 2008 Apr |
|
| Practical synthesis of 3beta-amino-5-cholestene and related 3beta-halides involving i-steroid and retro-i-steroid rearrangements. | 2009 Feb 5 |
|
| Solvent vapour detection with cholesteric liquid crystals--optical and mass-sensitive evaluation of the sensor mechanism. | 2010 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:13:56 GMT 2023
by
admin
on
Sat Dec 16 02:13:56 GMT 2023
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| Record UNII |
39EHZ05V39
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| Record Status |
Validated (UNII)
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| Record Version |
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1606197
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C060066
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DTXSID90883602
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213-004-4
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92850
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910-31-6
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39EHZ05V39
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CHOLESTERYL CHLORIDE
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39EHZ05V39
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2084
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DB14045
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