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10146-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10146-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10146-89:
(7*1)+(6*0)+(5*1)+(4*4)+(3*6)+(2*8)+(1*9)=71
71 % 10 = 1
So 10146-89-1 is a valid CAS Registry Number.

10146-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-2,3-diol

1.2 Other means of identification

Product number	-
Other names	3,6-Dioxo-cholestan

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:10146-89-1 SDS

10146-89-1Upstream product

10146-89-1Downstream Products

10146-89-1Relevant articles and documents

-

Cohen,Tsuji

, p. 1681 (1961)

Caputo et al.

, p. 619,623 (1975)

Hassner et al.

, p. 2632 (1969)

A NEW SYNTHESIS OF CIS-DIOL FROM OLEFIN USING IODINE-COPPER(II) ACETATE

Horiuchi, Akira,Satoh, Yasuo

, p. 1209 - 1210 (1988)

The reaction mixtures of 5α-cholest-2-ene with iodine and copper(II) acetate were converted with potassium hydroxide in methanol-water to give the more hindered 2β, 3β-diol in high yield.Cyclohexene and cycloheptene similarly gave the corresponding cis-diols in good yield.This new synthetic method afforded several advantage over the Prevost reaction.

King,Allbutt

, p. 49 (1967)

Regioselective enzymatic acylation of vicinal diols of steroids

Silva, M. Manuel Cruz,Riva, Sergio,Sá E Melo, M. Luisa

, p. 3065 - 3073 (2005)

Monoacylated derivatives of a complete set of 2,3- and 3,4-vicinal diols of steroids were prepared by regioselective lipase-catalysed transesterification reactions. The enzymes displayed different selectivities towards the vicinal diols depending on the configuration of the hydroxyl groups.

Synthesis and antiviral activity of sulfated and acetylated derivatives of 2β,3α-dihydroxy-5α-cholestane

Garrido Santos, Gustavo A.,Murray, Ana P.,Pujol, Carlos A.,Damonte, Elsa B.,Maier, Marta S.

, p. 125 - 132 (2007/10/03)

Five new steroid sulfates, sodium 2β,3α-dihydroxy-5α-cholestane 3-sulfate (6), sodium 2β,3α-dihydroxy-5α-cholestane 2-sulfate (7), disodium 2β,3α-dihydroxy-5α-cholestane disulfate (8), sodium 3α-acetoxy-2β-hydroxy-5α-cholestane 2-sulfate (12), and sodium

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CAS

10146-89-1