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(3beta)-cholest-5-en-3-yl 2-[4-(2-methylpropyl)phenyl]propanoate is a chemical compound that belongs to the family of cholesteryl esters. It is a derivative of cholesterol, with a 2-[4-(2-methylpropyl)phenyl]propanoate ester group attached to the 3-position of the cholesterol molecule. (3beta)-cholest-5-en-3-yl 2-[4-(2-methylpropyl)phenyl]propanoate has potential applications in the pharmaceutical and cosmetic industries due to its role in cholesterol metabolism and its ability to modulate cellular functions.

154394-15-7

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  • [(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] 2-[4-(2-methylpropyl)phenyl]propanoate

    Cas No: 154394-15-7

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154394-15-7 Usage

Uses

Used in Pharmaceutical Industry:
(3beta)-cholest-5-en-3-yl 2-[4-(2-methylpropyl)phenyl]propanoate is used as a pharmaceutical agent for its potential role in cholesterol metabolism and modulation of cellular functions. Its specific properties and potential uses would need to be further investigated and proven through research and testing.
Used in Cosmetic Industry:
(3beta)-cholest-5-en-3-yl 2-[4-(2-methylpropyl)phenyl]propanoate is used as a cosmetic ingredient for its potential role in modulating cellular functions and improving skin health. Its specific properties and potential uses would need to be further investigated and proven through research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 154394-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,3,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154394-15:
(8*1)+(7*5)+(6*4)+(5*3)+(4*9)+(3*4)+(2*1)+(1*5)=137
137 % 10 = 7
So 154394-15-7 is a valid CAS Registry Number.

154394-15-7Downstream Products

154394-15-7Relevant articles and documents

In search of safe pain relief: The analgesic and anti-inflammatory activity of phytosteryl ibuprofenates

Hernández-Flores, M. Elena,Torres-Valencia, J. Martín,Cari?o-Cortés, Raquel,Ortiz, Mario I.,López-Ruiz, Heraclio,Rojas-Lima, Susana,Cerda-García-Rojas, Carlos M.,Joseph-Nathan, Pedro

, (2019)

β-Sitosteryl (S)-ibuprofenate (2), stigmasteryl (S)-ibuprofenate (3), ergosteryl (S)-ibuprofenate (4), and cholesteryl (S)-ibuprofenate (5) were prepared in 70–75% yields by Steglich esterification and were characterized by 1D and 2D NMR, as well as by MS

Synthesis of the cholesteryl ester prodrugs cholesteryl ibuprofen and cholesteryl flufenamate and their formulation into phospholipid microemulsions

Murtha,Ando

, p. 1222 - 1228 (2007/10/02)

Phospholipid microemulsions have been suggested as a drug-delivery system for hydrophobic compounds. In this study hydrophobicity was achieved by derivatizing with cholesterol. Cholesteryl ibuprofen (3) and cholesteryl flufenamate (4) were synthesized. 3

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