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androstane-3,14-diol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98753-27-6

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98753-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98753-27-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,5 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98753-27:
(7*9)+(6*8)+(5*7)+(4*5)+(3*3)+(2*2)+(1*7)=186
186 % 10 = 6
So 98753-27-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H32O2/c1-12-7-10-19(21)15(12)5-6-16-17(19)4-3-13-11-14(20)8-9-18(13,16)2/h12-17,20-21H,3-11H2,1-2H3/t12-,13+,14-,15?,16-,17+,18-,19+/m0/s1

98753-27-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5β,14β-androstane-3β,14-diol

1.2 Other means of identification

Product number -
Other names (3S,5R,8R,9S,10S,13S,14S)-10,13-Dimethyl-hexadecahydro-cyclopenta[a]phenanthrene-3,14-diol

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:98753-27-6 SDS

98753-27-6Downstream Products

98753-27-6Relevant academic research and scientific papers

SYNTHESIS OF 3β-RHAMNOSYLOXY-5β,14β-ANDROSTAN-14-OL AND ITS 17-ACETOXY AND 17-HYDROXY DERIVATIVES

Kabat, Marek M.,Kurek, Alicja,Masnyk, Marek,Repke, Kurt R. H.,Schoenfeld, Werner,et al.

, p. 1711 - 1727 (2007/10/02)

The synthesis of 3β-rhamnosyloxy androstane derivatives 2a - 2e from 3a is described.Transformations in ring D involve introduction of the 14β-hydroxy group via epoxidation of the 14-ene (4a -> 6 -> 8a) or SeO2 oxidation of the 15-en-17-one (3a -> 8a).Red

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