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872002-72-7

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  • 6-[(4-{2-[4-(2-Methyl-2-propanyl)phenyl]-1H-benzimidazol-4-yl}-1- piperazinyl)methyl]quinoxaline

    Cas No: 872002-72-7

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872002-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 872002-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,0,0 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 872002-72:
(8*8)+(7*7)+(6*2)+(5*0)+(4*0)+(3*2)+(2*7)+(1*2)=147
147 % 10 = 7
So 872002-72-7 is a valid CAS Registry Number.

872002-72-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-[(4-{2-[4-(2-Methyl-2-propanyl)phenyl]-1H-benzimidazol-4-yl}-1- piperazinyl)methyl]quinoxaline

1.2 Other means of identification

Product number -
Other names -

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:872002-72-7 SDS

872002-72-7Downstream Products

872002-72-7Relevant articles and documents

Discovery of 6-({4-[2-(4-tert-Butylphenyl)-1H-benzimidazol-4-yl]piperazin- 1-yl}methyl)quinoxaline(WAY-207024): An orally active antagonist of the gonadotropin releasing hormone receptor (GnRH-R)

Pelletier, Jeffrey C.,Chengalvala, Murty V.,Cottom, Joshua E.,Feingold, Irene B.,Green, Daniel M.,Hauze, Diane B.,Huselton, Christine A.,Jetter, James W.,Kopf, Gregory S.,Lundquist, Joseph T.,Magolda, Ronald L.,Mann, Charles W.,Mehlmann, John F.,Rogers, John F.,Shanno, Linda K.,Adams, William R.,Tio, Cesario O.,Wrobel, Jay E.

supporting information; experimental part, p. 2148 - 2152 (2009/12/31)

A potent, highly insoluble, GnRH antagonist with a 2-phenyl-4- piperazinylbenzimidazole template and a quinoxaline-2,3-dione pharmacophore was modified to maintain GnRH antagonist activity and improve in vitro pharmaceutical properties. Structural changes

Processes for preparing gonadotropin releasing hormone receptor antagonists

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Page/Page column 18, (2008/06/13)

The present invention relates to methods of making Gonadotropin Releasing Hormone (“GnRH”) (also known as Leutinizing Hormone Releasing Hormone) receptor antagonists.

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