CAS 15455-80-8
:Cholest-5-en-3-ol (3β)-, 3-(hexyl carbonate)
Description:
Cholest-5-en-3-ol (3β)-, 3-(hexyl carbonate), also known by its CAS number 15455-80-8, is a chemical compound that belongs to the class of sterols, which are a subgroup of steroids. This substance features a cholesterol backbone, characterized by a four-ring core structure, with a hydroxyl group at the 3β position and a hexyl carbonate ester at the same position. The presence of the hexyl carbonate moiety contributes to its hydrophobic properties, influencing its solubility and interaction with biological membranes. The compound is typically used in biochemical research and may have applications in pharmaceuticals or cosmetic formulations due to its structural similarity to cholesterol, which plays a crucial role in cellular membrane integrity and fluidity. Its unique structure may also impart specific biological activities, making it a subject of interest in studies related to lipid metabolism and membrane dynamics. As with many sterols, it is important to consider its stability, reactivity, and potential interactions with other biomolecules in various environments.
Formula:C34H58O3
InChI:InChI=1S/C34H58O3/c1-7-8-9-10-22-36-32(35)37-27-18-20-33(5)26(23-27)14-15-28-30-17-16-29(25(4)13-11-12-24(2)3)34(30,6)21-19-31(28)33/h14,24-25,27-31H,7-13,15-23H2,1-6H3/t25-,27+,28+,29-,30+,31+,33+,34-/m1/s1
InChI key:InChIKey=FKPRFOWGXDAFNL-DYQRUOQXSA-N
SMILES:C[C@@]12[C@@]3([C@]([C@]4([C@](C)(CC3)[C@@]([C@@H](CCCC(C)C)C)(CC4)[H])[H])(CC=C1C[C@@H](OC(OCCCCCC)=O)CC2)[H])[H]
Synonyms:- 3β-Hexyloxycarbonyloxycholest-5-ene
- Cholest-5-en-3-ol (3β)-, 3-(hexyl carbonate)
- Cholest-5-en-3-ol (3β)-, hexyl carbonate
- Cholesterol n-hexyl carbonate
- Cholesterol, hexyl carbonate
- Cholesteryl hexyl carbonate
- Hexyl cholesteryl carbonate
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Found 3 products.
Cholesterol Hexyl Carbonate
CAS:Controlled Product<p>Cholesterol Hexyl Carbonate (C6HC) is a chiral organic compound with a unique conformation that enhances its adsorbing properties. C6HC is synthesized by reacting cholesterol with hexanoyl chloride in the presence of strong base and an inert solvent. The structural formula of this compound is shown in Figure 1.</p>Purity:Min. 95%
