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Propanamide, N-acetyl-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52220-93-6

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52220-93-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52220-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,2,2 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52220-93:
(7*5)+(6*2)+(5*2)+(4*2)+(3*0)+(2*9)+(1*3)=86
86 % 10 = 6
So 52220-93-6 is a valid CAS Registry Number.

52220-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-acetyl-2-methylpropanamide

1.2 Other means of identification

Product number -
Other names Propanamide,N-acetyl-2-methyl

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:52220-93-6 SDS

52220-93-6Relevant academic research and scientific papers

A bromine-catalysed free-radical oxidation of acetamides from primary and secondary alkylamines by H2O2

Bjorsvik,Fontana,Liguori,Minisci

, p. 523 - 524 (2007/10/03)

New procedures based on the oxidation by bromine-catalysed hydrogen peroxide in a two-phase system provide simple and cheap transformations of alkylamines to carbonyl derivatives (aldehydes, ketones, carboxylic acid, imides, lactams) through the corresponding acetamides.

The Nature of the Transition State in Amides Pyrolysis. The Rates of Pyrolysis of N-benzoyl and N-acetylpropanamide, N-benzoyl and N-acetyl-2-methylpropanamide, and N-thioacetylpropanamide

Al-Awadi, Nouria A.,Al-Omran, Fatima A.,Mathew, Tommy

, p. 1 - 6 (2007/10/02)

The rates of gas-phase elimination reactions of N-benzoyl and N-acetyl-propanamide and N-benzoyl and N-acetyl-2-methylpropanamide are measured and discussed.They undergo unimolecular first-order elimination reactions.The reactivities of N-benzoylamides have been compared with each other and with those of N-acetylamides.The kinetic data together with the product analysis reveals that, the statistical factor of the availability of β-hydrogen atoms for elimination as well as steric factor are obscured by polar factor in gas-phase elimination reactions of N-benzoylamides while the statistical factor rather than electronic effect operates in each of N-acetylamides.

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