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1219024-53-9

1219024-53-9

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1219024-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1219024-53-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,0,2 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1219024-53:
(9*1)+(8*2)+(7*1)+(6*9)+(5*0)+(4*2)+(3*4)+(2*5)+(1*3)=119
119 % 10 = 9
So 1219024-53-9 is a valid CAS Registry Number.

1219024-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(diphenylmethylene)hydrazino]benzonitrile

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:1219024-53-9 SDS

1219024-53-9Downstream Products

1219024-53-9Relevant articles and documents

PIPERIDINYLALKYLAMIDE DERIVATIVES HAVING MULTIMODAL ACTIVITY AGAINST PAIN

-

Page/Page column 114-115, (2017/11/10)

The present invention relates to piperidinylalkylamide derivatives having dual pharmacological activity towards both the sigma (σ) receptor and the μ-opioid receptor, to processes of preparation of such compounds, to pharmaceutical compositions comprising

Two-step synthesis of substituted 3-aminoindazoles from 2-bromobenzonitriles

Lefebvre, Valerie,Cailly, Thomas,Fabis, Frederic,Rault, Sylvain

supporting information; experimental part, p. 2730 - 2732 (2010/07/08)

A general two-step synthesis of substituted 3-aminoindazoles from 2-bromobenzonitriles involving a palladium-catalyzed arylation of benzophenone hydrazone followed by an acidic deprotection/cyclization sequence is described. This procedure offers a general and efficient alternative to the typical S NAr reaction of hydrazine with o-fluorobenzonitriles.

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