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53502-23-1

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53502-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53502-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,0 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53502-23:
(7*5)+(6*3)+(5*5)+(4*0)+(3*2)+(2*2)+(1*3)=91
91 % 10 = 1
So 53502-23-1 is a valid CAS Registry Number.

53502-23-1SDS

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 4-acetamido-3-nitrobenzophenone

1.2 Other means of identification

Product number -
Other names 4-BENZOYL-2-NITROACETANILIDE

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:53502-23-1 SDS

53502-23-1Relevant articles and documents

Electron Impact Ionized Benzoylnitroanilines and their N-Alkyl and N-Acyl Derivatives

Ayyangar, N. R.,Sudalai, A.,Daniel, Thomas

, p. 633 - 635 (2007/10/02)

The behaviour of some benzoylnitroanilines and their derivatives under electron impact ionization was investigated by means of low-resolution mass spectrometry.Some characteristic rearrangement processes are discussed.

Acyl Trimethylsilyl Polyphosphates as Activated Esters in Acylation Reactions

Rao, C. Someswara,Rambabu, M.,Srinivasan, P. S.

, p. 407 - 411 (2007/10/02)

The preparation and application of a new class of activated esters, acyl trimethylsilyl polyphosphates, are described.These complexes, prepared by the reaction of trimethylsilyl carboxylates with phosphorus pentoxide, are versatile acylating agents under relatively mild conditions.Sodium or potassium halides and imidazole are very effective catalysts leading to the in situ generation of reactive acyl halides and acyl imidazolides.Amines, amides, alcohols and phenols, p-thiocresol, carboxylic acids and trimethylsilyl carboxylates, and hexamethyldisilazane have been acylated to give high yields of amides, imides, esters, thioesters, anhydrides and nitriles, respectively.

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