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(22R)-5α-Lanosta-8,24-diene-3β,22-diol is a chemical compound belonging to the lanosterol family. It is a sterol, a type of lipid molecule that plays a crucial role in the structure and function of cell membranes. (22R)-5α-Lanosta-8,24-diene-3β,22-diol features a 3β,22-diol group and a double bond at the 8,24 position, derived from lanosterol, which is a precursor in cholesterol biosynthesis. The 5α configuration denotes the molecule's stereochemistry, which is significant for its biological activity. (22R)-5α-Lanosta-8,24-diene-3β,22-diol holds potential in pharmaceutical and medical research, serving as a precursor for the synthesis of steroidal drugs or as a target for drug development.

35963-37-2

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35963-37-2 Usage

Uses

Used in Pharmaceutical Industry:
(22R)-5α-Lanosta-8,24-diene-3β,22-diol is used as a precursor in the synthesis of steroidal drugs for its ability to be chemically modified to produce a variety of medicinal compounds with diverse therapeutic applications.
Used in Medical Research:
(22R)-5α-Lanosta-8,24-diene-3β,22-diol is used as a target for drug development due to its potential role in cholesterol biosynthesis and its unique structural features, which may lead to the discovery of new therapeutic agents or treatments for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 35963-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,6 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35963-37:
(7*3)+(6*5)+(5*9)+(4*6)+(3*3)+(2*3)+(1*7)=142
142 % 10 = 2
So 35963-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O2/c1-19(2)9-11-24(31)20(3)21-13-17-30(8)23-10-12-25-27(4,5)26(32)15-16-28(25,6)22(23)14-18-29(21,30)7/h9,20-21,24-26,31-32H,10-18H2,1-8H3/t20-,21+,24+,25?,26-,28+,29+,30-/m0/s1

35963-37-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,10S,13R,14R,17R)-17-[(2S,3R)-3-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

1.2 Other means of identification

Product number -
Other names 3beta,22-dihydroxylanosta-8,24-dien-7-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35963-37-2 SDS

35963-37-2Downstream Products

35963-37-2Relevant academic research and scientific papers

The stereospecific synthesis of inotodiol 3β, 22R-dihydroxylanosta-8,24-diene

Poyser,de Reinach Hirtzbach,Ourisson

, p. 977 - 986 (1974)

Inotodiol 1a has been stereospecifically synthesised from lanosterol in six steps and Horeau's method utilised to demonstrate the R-configuration at C-22.

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