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165387-78-0

165387-78-0

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165387-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 165387-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,3,8 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 165387-78:
(8*1)+(7*6)+(6*5)+(5*3)+(4*8)+(3*7)+(2*7)+(1*8)=170
170 % 10 = 0
So 165387-78-0 is a valid CAS Registry Number.

165387-78-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-phenylpyridin-3-amine

1.2 Other means of identification

Product number -
Other names 2-chloro-3-amino-4-phenylpyridine

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:165387-78-0 SDS

165387-78-0Relevant articles and documents

Antagonists of inhibitor of apoptosis proteins based on thiazole amide isosteres

Cohen, Frederick,Koehler, Michael F.T.,Bergeron, Philippe,Elliott, Linda O.,Flygare, John A.,Franklin, Matthew C.,Gazzard, Lewis,Keteltas, Stephen F.,Lau, Kevin,Ly, Cuong Q.,Tsui, Vickie,Fairbrother, Wayne J.

scheme or table, p. 2229 - 2233 (2010/06/15)

A series of IAP antagonists based on thiazole or benzothiazole amide isosteres was designed and synthesized. These compounds were tested for binding to the XIAP-BIR3 and ML-IAP BIR using a fluorescence polarization assay. The most potent of these compound

INHIBITORS OF IAP

-

, (2008/06/13)

The invention provides novel inhibitors of IAP that are useful as therapeutic agents for treating malignancies where the compounds have the general formula (I): wherein Q, X1, X2, Y, Z1, Z2, Z3, Z4, R1, R2, R3, R3', R4, R4', R5, R6, R6' and n are as described herein.

Method for preparing 3-amino-2-chloro-4-alkylpyridine or-4-arylpyridine

-

, (2008/06/13)

The present invention relates to a new process for preparing 3-amino-2-chloro-4-alkyl- or -4-aryl-pyridines on an industrial scale.

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