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155142-81-7

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155142-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155142-81-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,1,4 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155142-81:
(8*1)+(7*5)+(6*5)+(5*1)+(4*4)+(3*2)+(2*8)+(1*1)=117
117 % 10 = 7
So 155142-81-7 is a valid CAS Registry Number.

155142-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-bromo-N-butyl-N-methylundecanamide

1.2 Other means of identification

Product number -
Other names N-Butyl-N-methyl-11-bromoundecanamide

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:155142-81-7 SDS

155142-81-7Relevant articles and documents

STEROIDS FOR CANCER TREATMENT

-

Page/Page column 31, (2010/02/13)

The present invention relates to novel compounds which are 7α-substituted 17-alkylene-16α-hydroxy steroidal estrogens. This invention specifically relates to estrogen derivatives which contain 7α-substituents and which exhibit anti-estrogenic properties. The present invention also relates to use of said compounds as a medicament, and for the treatment of estrogen dependent disorders, a pharmaceutical composition comprising one or more of said compounds and a method of treatment.

An expeditious route to 7α-substituted estradiol derivatives

Tedesco, Rosanna,Katzenellenbogen, John A.,Napolitano, Elio

, p. 7997 - 8000 (2007/10/03)

6-Ketoestradiol derivatives are converted in 7α-alkyl substituted estradiol derivatives selectively by alkylation of the generated enolate followed by deoxygenation-deprotection with BF3·Et2O/Et3SiH.

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