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(R)-5-(benzoyloxy)-3-(1-methylethyl)pentan-1-ol is a chiral compound derived from pentan-1-ol, featuring a benzoyloxy group at the 5th carbon and an isopropyl group at the 3rd carbon. Its unique structure, with a stereocenter at the 5th carbon, results in two enantiomeric forms, (R) and (S). (R)-5-(benzoyloxy)-3-(1-methylethyl)pentan-1-ol is of significant interest in the fields of pharmaceutical and chemical industries due to its versatile applications and useful properties.

100431-73-0

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100431-73-0 Usage

Uses

Used in Pharmaceutical Industry:
(R)-5-(benzoyloxy)-3-(1-methylethyl)pentan-1-ol is used as a building block for the synthesis of various pharmaceutical drugs. Its unique structure and chirality make it a valuable component in the development of new medications, contributing to the advancement of drug discovery and design.
Used in Chemical Industry:
In the chemical industry, (R)-5-(benzoyloxy)-3-(1-methylethyl)pentan-1-ol is utilized for the synthesis of a range of organic compounds. Its versatility and reactivity in chemical reactions allow for the creation of diverse chemical products, further expanding its applications and importance in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 100431-73-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,3 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100431-73:
(8*1)+(7*0)+(6*0)+(5*4)+(4*3)+(3*1)+(2*7)+(1*3)=60
60 % 10 = 0
So 100431-73-0 is a valid CAS Registry Number.

100431-73-0Relevant academic research and scientific papers

Synthesis of Enantiomerically Pure 24-Alkylsterol Side Chains, in Both Enantiomeric Forms, Starting from (R)-(+)-Limonene

Nicotra, Francesco,Panza, Luigi,Ronchetti, Fiamma,Russo, Giovanni,Toma, Lucio

, p. 1272 - 1276 (2007/10/02)

Three couples of enentiomeric synthons corresponding to six 24-alkylsterol side chains, (R)- and (S)-1-bromo-3,4-dimethylpentane, (R)-and (S)-1-bromo-3-ethyl-4-methylpentane, and (R)- and (S)-5-(acetyloxy)-1-bromo-3-(1-methylethyl)pentane, were synthesize

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