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1H-Pyrazole-4,5-dione, 3-methyl-1-(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60759-53-7

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60759-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60759-53-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,5 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 60759-53:
(7*6)+(6*0)+(5*7)+(4*5)+(3*9)+(2*5)+(1*3)=137
137 % 10 = 7
So 60759-53-7 is a valid CAS Registry Number.

60759-53-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methyl-2-(4-nitrophenyl)pyrazole-3,4-dione

1.2 Other means of identification

Product number -
Other names 3-methyl-1-(4-nitrophenyl)-1H-pyrazole-4,5-dione

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:60759-53-7 SDS

60759-53-7Relevant academic research and scientific papers

Syntheses of gem-dinitro heterocyclic compounds, their ring-opening reactions and transformations into indoles, indazoles and benzoxazinones

Bergman, Jan,Bergman, Solveig,Brimert, Thomas

, p. 10447 - 10466 (2007/10/03)

The synthesis of some novel 3,3,5,7-tetranitrooxindoles and 4,4- dinitropyrazol-5-ones and their behaviour towards various nucleophiles and electrophiles are reported. Reactions with hydroxide ions or secondary amines produced salts of e.g. 2-amino-3,5-dinitrophenyldinitromethane, which subsequently could be further transformed into indazoles, indoles or benzoxazinones depending upon substrate and conditions used. Mechanisms are discussed.

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