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82544-13-6

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82544-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82544-13-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,5,4 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82544-13:
(7*8)+(6*2)+(5*5)+(4*4)+(3*4)+(2*1)+(1*3)=126
126 % 10 = 6
So 82544-13-6 is a valid CAS Registry Number.

82544-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6β-epoxy-7β-hydroxy-15β,16β-methylene-3β-pivaloyloxy-5β-androstan-17-one

1.2 Other means of identification

Product number -
Other names 5,6β-epoxy-7β-hydroxy-15β,16β-methylen-3β-pivaloyloxy-5β-androstan-17-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:82544-13-6 SDS

82544-13-6Relevant articles and documents

Process for the preparation of Drospirenone

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Page/Page column 7; 9; 28, (2009/02/10)

A process for the preparation of Drospirenone (I) according to the following scheme wherein the substituent R is defined in the description. The process improves the product yield and purity by reducing the formation of undesired side-products and is particularly convenient for industrial-scale manufacturing.

Process for preparing 3β,7β-dihydroxy-Δ5 -steroids

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, (2008/06/13)

A process for preparing a 3β,7β-dihydroxy-Δ5 steroid of the formula STR1 wherein Q is STR2 and R1 is hydrogen, trimethylacetyl, tert-butyldimethylsilyl, dimethyl-2-(3-methylbutyl)silyl or tribenzylsilyl, comprises fermenting a 3β-hydroxy-Δ5 -steroid of the formula STR3 wherein Q is as defined above, and R2 is hydrogen or alkanoyl of 2-6 carbon atoms, with a culture of Botryodiplodia malorum to obtain the corresponding 3β,7β-dihydroxy-Δ5 -steroid; and, optionally, reacting the resultant product with trimethylacetic anhydride, tert-butyldimethylsilyl chloride, dimethyl-2-(3-methylbutyl)silyl chloride, or tribenzylsilyl chloride.

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