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9,11-seco-3,6,11-trihydroxycholest-7-en-9-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

143625-39-2

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143625-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143625-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,2 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 143625-39:
(8*1)+(7*4)+(6*3)+(5*6)+(4*2)+(3*5)+(2*3)+(1*9)=122
122 % 10 = 2
So 143625-39-2 is a valid CAS Registry Number.
InChI:InChI=1/C27H46O4/c1-17(2)7-6-8-18(3)21-9-10-22(26(21,4)13-14-28)20-16-24(30)23-15-19(29)11-12-27(23,5)25(20)31/h16-19,21-24,28-30H,6-15H2,1-5H3/t18-,19?,21-,22?,23?,24?,26-,27+/m1/s1

143625-39-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (8aS)-4,6-dihydroxy-2-[(2R,3R)-2-(2-hydroxyethyl)-2-methyl-3-[(2R)-6-methylheptan-2-yl]cyclopentyl]-8a-methyl-4,4a,5,6,7,8-hexahydronaphthalen-1-one

1.2 Other means of identification

Product number -
Other names 9,11-Seco-3beta,6alpha,11-trihydroxy-5alpha-cholest-7-en-9-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:143625-39-2 SDS

143625-39-2Downstream Products

143625-39-2Relevant academic research and scientific papers

Two new 9,11-secosterols from the marine sponge Spongia officinalis. Synthesis of 9,11-seco-3β,6α,11-trihydroxy-5α-cholest-7-en-9-one

Migliuolo, Anna,Piccialli, Vincenzo,Sica, Donato

, p. 344 - 347 (1992)

Two new 9,11-secosterol, 9,11-seco-3β,6α,11-trihydroxy-5α-cholest-7-en-9-one (2) and 9,11-seco-3β,6α,11-trihydroxy-24-methylene-5α-cholest-7-en-9-one (3), have been isolated from the marine sponge Spongia officinalis and their structures elucidated by analysis of spectral data including 1H nuclear magnetic resonance correlation spectroscopy (COSY) experiments.Partial synthesis of 2 starting from 3β,6α-dihydroxy-9-oxo-9,11-seco-5α-cholest-7-en-11-al (1) confirmed the structure assignment. Keywords: sterols; 9,11-secosterols; 9,11-seco-3β,6α,11-trihydroxy-5α-cholest-7-en-9-one; 9,11-seco-3β,6α,11-trihydroxy-24-methylene-5α-cholest-7-en-9-one; synthesis; 1H nuclear magnetic resonance; 13C nuclear magnetic resonance; two-dimensional nuclear magnetic resonance correlation spectroscopy

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