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210536-90-6

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210536-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210536-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,5,3 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 210536-90:
(8*2)+(7*1)+(6*0)+(5*5)+(4*3)+(3*6)+(2*9)+(1*0)=96
96 % 10 = 6
So 210536-90-6 is a valid CAS Registry Number.

210536-90-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3-methoxyphenyl) benzophenone hydrazone

1.2 Other means of identification

Product number -
Other names N-Benzhydrylidene-N'-(3-methoxy-phenyl)-hydrazine

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:210536-90-6 SDS

210536-90-6Downstream Products

210536-90-6Relevant articles and documents

ErbB RECEPTOR INHIBITORS AS ANTI-TUMOR AGENTS

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Page/Page column 167; 168, (2021/09/17)

Provided herein are novel compounds as inhibitors of type I receptor tyrosine kinases, the pharmaceutical compositions comprising one or more of the compounds and salts thereof as an active ingredient, and the use of the compounds and salts thereof in the treatment of hyperproliferative diseases, such as cancer and inflammation, in mammals and especially in humans.

Highly reactive, general, and long-lived catalysts for coupling heteroaryl and aryl chlorides with primary nitrogen nucleophiles

Shen, Qilong,Shekhar, Shashank,Stambuli, James P.,Hartwig, John F.

, p. 1371 - 1375 (2007/10/03)

Resisting pathways for decomposition followed by palladium complexes of monodentate ligands is one characteristic of the highly reactive but long-lived catalyst generated from the Josiphos ligand L and palladium. It catalyzes under mild conditions the coupling of primary amines with chloropyridines and chloroarenes in high yield with low catalyst loadings (see scheme).

A palladium-catalyzed strategy for the preparation of indoles: A novel entry into the Fischer indole synthesis

Wagaw,Yang,Buchwald

, p. 6621 - 6622 (2007/10/03)

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