Description

Cholest-5-en-3-beta-yl cinnamate (CAS: 1990-11-0) is a high-purity steroidal ester compound with the molecular formula C₃₆H₅₂O₂. This specialized chemical is derived from cholesterol and cinnamic acid, offering unique properties for advanced research and industrial applications. It is widely utilized in pharmaceutical development, material science, and biochemical studies due to its steroidal backbone and cinnamate functional group. Our product is rigorously tested for purity and consistency, ensuring optimal performance in your experiments. Available in various quantities to meet both laboratory and bulk industrial demands, this compound is ideal for researchers seeking reliable, high-quality steroidal derivatives.

Properties

• CAS Number: 1990-11-0
• Complexity: 878
• IUPAC Name: [(3S,8S,9S,10R,13R,14S,17R)-17-[(1R)-1,5-dimethylhexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (E)-3-phenylprop-2-enoate
• InChI: InChI=1S/C36H52O2/c1-25(2)10-9-11-26(3)31-17-18-32-30-16-15-28-24-29(38-34(37)19-14-27-12-7-6-8-13-27)20-22-35(28,4)33(30)21-23-36(31,32)5/h6-8,12-15,19,25-26,29-33H,9-11,16-18,20-24H2,1-5H3/b19-14+/t26-,29+,30+,31-,32+,33+,35+,36-/m1/s1
• InChI Key: FESYLMLHRKCTFF-MFLJIVHPSA-N
• Exact Mass: 516.396730897
• Molecular Formula: C36H52O2
• Molecular Weight: 516.8
• SMILES: C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)OC(=O)/C=C/C5=CC=CC=C5)C)C
• Topological: 26.3
• Monoisotopic Mass: 516.396730897
• Synonyms: Cholest-5-en-3-beta-yl cinnamate, 1990-11-0, Cholest-5-en-3-ol (3beta)-, 3-(3-phenyl-2-propenoate), EINECS 217-869-9, DTXSID401014583, Cholest-5-en-3-ol (3beta)-, 3-phenyl-2-propenoate, DTXCID401437147, Cholest-5-en-3-ol (3.beta.)-, 3-(3-phenyl-2-propenoate), 217-869-9, Cholesterol trans-Cinnamate, Cholesteryl cinnamate, 50305-81-2, trans-Cinnamic Acid Cholesterol Ester, [(3S,8S,9S,10R,13R,14S,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-yl] (E)-3-phenylprop-2-enoate, Cholest-5-en-3-ol (3.beta.)-, 3-phenyl-2-propenoate, SCHEMBL162269, 5-Cholesten-3.beta.-ol cinnamate, AKOS025295384, FC61963, NS00045438, (E)-3.beta.-(3-Phenylpropenoyloxy)cholest-5-ene, Cholest-5-en-3-yl (2E)-3-phenyl-2-propenoate #

Cholest-5-en-3-beta-yl cinnamate is primarily used in pharmaceutical research for studying steroidal interactions and drug delivery systems. It serves as a key intermediate in synthesizing novel bioactive compounds with potential therapeutic applications. Additionally, this ester is explored in material science for liquid crystal formulations and polymer modifications. Its unique structure makes it valuable for investigating lipid membranes and sterol-protein interactions in biochemistry.

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