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49756-87-8

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49756-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49756-87-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,7,5 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 49756-87:
(7*4)+(6*9)+(5*7)+(4*5)+(3*6)+(2*8)+(1*7)=178
178 % 10 = 8
So 49756-87-8 is a valid CAS Registry Number.

49756-87-8SDS

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 17α-ethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol

1.2 Other means of identification

Product number -
Other names (3R,5R,8R,9S,10S,17R)-17-Ethyl-10,17-dimethyl-2,3,4,5,6,7,8,9,10,11,12,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

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:49756-87-8 SDS

49756-87-8Downstream Products

49756-87-8Relevant articles and documents

Clinical Analysis on Steroids. XII. Occurrence of D-Homoannulation during the Hot Acid Hydrolysis of 5β-Pregnane-3α,20α-diol Disulfate

Yoshizawa, Itsuo,Nagata, Kyoko,Oh'uchi, Ryoko,Itoh, Shinji,Kanaiwa, Yoshio,Amiya, Takashi

, p. 87 - 96 (1980)

Two D-homosteroids were isolated from the hydrolyzate of 5β-pregnane-3α,20α-diol disulfate (II) when it was refluxed in 3N hydrochloric acid.The structures of these steroids have been elucidated as 17α-methyl-D-homo-5β-androstane-3α,17aβ-diol (VI) and 17α-methyl-17aβ-chloro-D-homo-5β-androstan-3α-ol (VIII) by instrumental analyses.The former was identical with a synthetic specimen derived from 5β-pregnane-3α,20β-diol disulfate (IV) by uranediol rearrangement.The main hydrolyzates obtained were 17α-ethyl-17β-methyl-18-nor-5β-androst-13-en-3α-ol (V) and 5β-pregnane-3α-20α-diol (III).

Isolation and structural elucidation of the degradation products of pregnanediol disulfate obtained by hot acid hydrolysis (clinical analysis on steroids. XXI)

Yoshizawa,Oh'uchi,Nagata,et al.

, p. 2474 - 2486 (2007/10/02)

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