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34635-42-2

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34635-42-2 Usage

Chemical Properties

Yellow Solid

Uses

Intermediate in the preparation of Testosterone metabolties.

Check Digit Verification of cas no

The CAS Registry Mumber 34635-42-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,3 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 34635-42:
(7*3)+(6*4)+(5*6)+(4*3)+(3*5)+(2*4)+(1*2)=112
112 % 10 = 2
So 34635-42-2 is a valid CAS Registry Number.

34635-42-2SDS

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 [(3R,8R,9S,10R,13S)-17-acetyloxy-10,13-dimethyl-2,3,4,7,8,9,11,12-octahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names Androsta-5,14,16-triene-3|A,17-diol,Diacetate

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:34635-42-2 SDS

34635-42-2Relevant articles and documents

Synthesis of 14,16-dien-17-yl acetates of androstane series. NMR and mass spectrometry data

Baranovskii,Bolibrukh,Gromak

experimental part, p. 1877 - 1885 (2012/01/07)

On the basis of dehydroepiandrosterone through the δ14- and δ 15-androst-17-ones a series of androsta-14,16-dienyl acetates was obtained, the key compounds in the synthesis of 14-substituted steroids. By the methods of two-dimensional NMR spectroscopy the structure of compounds was proved and a full assignment of signals in the 1H and 13C NMR spectra was performed. With the use of tandem mass spectrometry the main directions of fragmentation of protonated molecules of the synthesized ketones and dienyl acetates were studied.

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