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84871-06-7

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84871-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84871-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,7 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84871-06:
(7*8)+(6*4)+(5*8)+(4*7)+(3*1)+(2*0)+(1*6)=157
157 % 10 = 7
So 84871-06-7 is a valid CAS Registry Number.

84871-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (24S,25S)-24,26-cyclocholesta-5,22E-dien-3β-ol, glaucasterol

1.2 Other means of identification

Product number -
Other names (3S,8S,9S,10R,13R,14S,17R)-10,13-Dimethyl-17-[(E)-(R)-1-methyl-3-((1S,2S)-2-methyl-cyclopropyl)-allyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

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:84871-06-7 SDS

84871-06-7Upstream product

84871-06-7Downstream Products

84871-06-7Relevant articles and documents

STEREOSELECTIVE SYNTHESIS OF SIDE CHAIN OF GLAUCASTEROL USING PALLADIUM (0) CATALYST.

Genet, J. P.,Gaudin, J. M.

, p. 5315 - 5320 (2007/10/02)

A stereoselective synthesis of glaucasterol 1 with vinylic cyclopropane on the side chain, has been developed using palladium (0) catalyst and gave complete chirality transfer from C22 of benzoate 15 to C24 of glaucasterol 1.

STEREOCONTROLLED SYNTHESIS AND DETERMINATION OF THE C-24 AND 25 STEREOCHEMISTRY OF GLAUCASTEROL

Fujimoto, Yoshinori,Kimura, Miki,Terasawa, Takeshi,Khalifa, Fathy A. M.,Ikekawa, Nobuo

, p. 1805 - 1808 (2007/10/02)

(24S,25S)- and (24R,25R)-24,26-Cyclocholesta-5,22E-dien-3β-ols (1a and 1b) were synthesized stereoselectively.Their 1H NMR comparison with natural glaucasterol (1) allowed to conclude that 1 possesses 24S, 25S stereochemistry.

MINOR AND TRACE STEROLS IN MARINE INVERTEBRATES 38 : ISOLATION, STRUCTURE ELUCIDATION AND PARTIAL SYNTHESIS OF PAPAKUSTEROL, A NEW BIOSYNTHETICALLY UNUSUAL MARINE STEROL WITH A CYCLOPROPYL-CONTAINING SIDE CHAIN.

Bonini, Carlo,Kinnel, Robin B.,Li, Michael,Scheuer, Paul J.,Djerassi, Carl

, p. 277 - 280 (2007/10/02)

A new cyclopropyl-containing sterol papakusterol (22-dehydro-24,26-cyclocholesterol), arising by a hitherto unknown biosynthetic process, was isolated from six "deep sea" gorgonians and its structure alucidated by 1H-NMR analysis and partial synthesis.Traces of the corresponding Δ5,7-diene have also been encountered.

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