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10329-87-0

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10329-87-0 Usage

Type of Compound

Synthetic derivative of estrogen

Classification

Steroid, estrogenic hormone

Usage

Scientific research tool for studying estrogen receptor binding and estrogenic activity

Activity

Similar estrogenic activity to natural estradiol

Purpose

Comparing effects of different estrogenic compounds on biological systems

Applications

Development of new drugs for hormone replacement therapy, study of estrogen-related diseases

Check Digit Verification of cas no

The CAS Registry Mumber 10329-87-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,2 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 10329-87:
(7*1)+(6*0)+(5*3)+(4*2)+(3*9)+(2*8)+(1*7)=80
80 % 10 = 0
So 10329-87-0 is a valid CAS Registry Number.

10329-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 13-methyl-17-sulfanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-ol

1.2 Other means of identification

Product number -
Other names Testosterone isobutyrate

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:10329-87-0 SDS

10329-87-0Relevant articles and documents

Mercaptans from thioketals: Cyclododecyl mercaptan

Wilson,Georgiadis

, p. 74 - 74 (2017/05/17)

-

Metalation of 1,3-Dithiolanes. Mercaptan Synthesis and Carbonyl Transposition

Wilson, Stephen R.,Georgiadis, Gregory M.,Khatri, Hiralal N.,Bartmess, John E.

, p. 3577 - 3583 (2007/10/02)

The reaction of 1,3-dithiolanes with n-butyllithium results in fragmentation to the corresponding thiocarbonyl compound followed by furhter reaction with n-butyllithium.All four types of thiocarbonyl reactions are observed: reduction, S-addition, C-addition, double addition.Synthetic applications of this reaction for the synthesis of secondary mercaptans and 1,2-carbonyl transposition (23 -> 24a-c) are described.

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