Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C34H50O2 |
Molecular Weight | 490.7596 |
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](CC[C@]4(C)[C@@]3([H])CC[C@]12C)OC(=O)C5=CC=CC=C5)[C@H](C)CCCC(C)C
InChI
InChIKey=UVZUFUGNHDDLRQ-LLHZKFLPSA-N
InChI=1S/C34H50O2/c1-23(2)10-9-11-24(3)29-16-17-30-28-15-14-26-22-27(36-32(35)25-12-7-6-8-13-25)18-20-33(26,4)31(28)19-21-34(29,30)5/h6-8,12-14,23-24,27-31H,9-11,15-22H2,1-5H3/t24-,27+,28+,29-,30+,31+,33+,34-/m1/s1
Molecular Formula | C34H50O2 |
Molecular Weight | 490.7596 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 8 / 8 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/11625121
Sources: https://www.ncbi.nlm.nih.gov/pubmed/11625121
There is no information in the scientific literature related to the biological and pharmacological properties of cholesteryl benzoate. Nevertheless, it is known, that initially it was used in some thermochromic liquid crystals. In addition, it can be used as an intermediate of vitamin D3 production, and in make-ups.
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:08:30 GMT 2023
by
admin
on
Fri Dec 15 15:08:30 GMT 2023
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Record UNII |
N09H13SHLB
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Record Status |
Validated (UNII)
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Record Version |
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SUB13347MIG
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DTXSID10897509
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N09H13SHLB
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604-32-0
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2723613
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210-064-3
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100000080080
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CHOLESTERYL BENZOATE
Created by
admin on Fri Dec 15 15:08:30 GMT 2023 , Edited by admin on Fri Dec 15 15:08:30 GMT 2023
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C029808
Created by
admin on Fri Dec 15 15:08:30 GMT 2023 , Edited by admin on Fri Dec 15 15:08:30 GMT 2023
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