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782492-17-5

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782492-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 782492-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,2,4,9 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 782492-17:
(8*7)+(7*8)+(6*2)+(5*4)+(4*9)+(3*2)+(2*1)+(1*7)=195
195 % 10 = 5
So 782492-17-5 is a valid CAS Registry Number.

782492-17-5SDS

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 3-{(3S,4S)-1-[(1R)-3-Isopropyl-3-{[6-(trifluoromethyl)-2H-1,3-ben zoxazin-3(4H)-yl]carbonyl}cyclopentyl]-3-methyl-4-piperidinyl}ben zoic acid

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:782492-17-5 SDS

782492-17-5Downstream Products

782492-17-5Relevant articles and documents

Discovery of a potent and orally bioavailable CCR2 and CCR5 dual antagonist

Pasternak, Alexander,Goble, Stephen D.,Struthers, Mary,Vicario, Pasquale P.,Ayala, Julia M.,Di Salvo, Jerry,Kilburn, Ruth,Wisniewski, Thomas,Demartino, Julie A.,Mills, Sander G.,Yang, Lihu

scheme or table, p. 14 - 18 (2010/11/04)

This report describes the discovery of a potent, orally bioavailable CC chemokine receptor 2 (CCR2) antagonist which, while optimized for CCR2 potency, also had potent CC chemokine receptor 5 (CCR5) activity.

BENZOXAZINYL-AMIDOCYCLOPENTYL-HETEROCYCLIC MODULATORS OF CHEMOKINE RECEPTORS

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Page 64, (2010/02/09)

Cyclopentyl compounds linked to a benzoxazinyl group through an amido moiety utilizing the ring nitrogen of the benzoxazine, and further substituted with a heterocyclic moiety, such compounds represented by formula (I): which are used to modulate the CCR-

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