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93065-62-4

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93065-62-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93065-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,0,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 93065-62:
(7*9)+(6*3)+(5*0)+(4*6)+(3*5)+(2*6)+(1*2)=134
134 % 10 = 4
So 93065-62-4 is a valid CAS Registry Number.

93065-62-4SDS

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 [4-(4-nitrobenzoyl)piperazin-1-yl]-(4-nitrophenyl)methanone

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:93065-62-4 SDS

93065-62-4Relevant articles and documents

Oxidative amidation of benzaldehyde using a quinone/DMSO system as the oxidizing agent

Mejía-Farfán, Itzel,Solís-Hernández, Manuel,Navarro-Santos, Pedro,Contreras-Celedón, Claudia A.,Cortés-García, Carlos Jesus,Chacón-García, Luis

, p. 18265 - 18270 (2019/07/03)

An efficient transition-metal-based heterogeneous catalyst free procedure for obtaining the oxidative amidation of benzaldehyde using quinones as oxidizing agents in low molar proportions is described here. Pyrrolylquinones (PQ) proved to be more suitable

Reaction of piperazine with trimethylacetic arylcarboxylic anhydride; a convenient method for preparing monoacylated piperazine derivatives

Lai,Wang,Luh

, p. 361 - 363 (2007/10/03)

A series of monosubstituted piperazine derivatives were obtained by the reaction of piperazine with trimethylacetic arylcarboxylic anhydrides in good yields, which were prepared in situ from arylcarboxylic acid with trimethylacetyl chloride in the presence of triethylamine.

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