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120982-79-8

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120982-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120982-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,9,8 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120982-79:
(8*1)+(7*2)+(6*0)+(5*9)+(4*8)+(3*2)+(2*7)+(1*9)=128
128 % 10 = 8
So 120982-79-8 is a valid CAS Registry Number.

120982-79-8SDS

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 ethyl 2-(4,5-diphenylpyrazol-1-yl)acetate

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole-1-aceticacid,3,4-diphenyl-,ethyl ester

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:120982-79-8 SDS

120982-79-8Upstream product

120982-79-8Relevant articles and documents

N-(heterocycle)alkyl)-1H-pyrazole-1-alkanamides as antiarrhythmic agents, compositions and use

-

, (2008/06/13)

N-[(heterocycle)alkyl]-3,4 (or 4,5)-diaryl-1H-pyrazole-1-acetamides and pyrazole-1-propanamides, useful for treating cardiac arrhythmias in mammals, are prepared by reacting a lower-alkyl ester of pyrazole-1-acetic or propanoic acid with an appropriate (heterocycle-alkyl) amine or by reacting a pyrazole-1-acetic or propanoic acid with an appropriate (heterocycle-alkyl)amine.

1H-pyrazole-1-alkanamides, antiarrhythmic compositions and use

-

, (2008/06/13)

N-[(disubstituted amino)alkyl]-3,4 (or 4,5)-diaryl-1H-pyrazole-1-acetamides and pyrazole-1-propanamides, useful for treating cardiac arrhythmias in mammals, are prepared by reacting a lower-alkyl ester of pyrazole-1-acetic or propanoic acid with an appropriate diamine or by reacting a lower-alkyl ester of a pyrazole-1-acetic or propanoic acid with an ω-aminoalkanol, followed by activation of the alcohol and displacement by an appropriate amine.

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