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Carbamoperoxoic acid, dimethyl-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42930-04-1

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42930-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42930-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,9,3 and 0 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42930-04:
(7*4)+(6*2)+(5*9)+(4*3)+(3*0)+(2*0)+(1*4)=101
101 % 10 = 1
So 42930-04-1 is a valid CAS Registry Number.

42930-04-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl dimethylcarbamoperoxoate

1.2 Other means of identification

Product number -
Other names Dimethyl-peroxycarbamidsaeure-tert-butylester

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:42930-04-1 SDS

42930-04-1Relevant academic research and scientific papers

PERCARBAMATE DE t-BUTYLE ET SES DERIVES N-ALKYLES, N,N-DIALKYLES ET N-AZACYCLANIQUES: PREPARATION ET THERMOLYSE EN SOLUTION

Buorgeois, M. J.,Campagnole, M.,Filliatre, C.,Maillard, B.,Manigand, C.,et al.

, p. 3569 - 3577 (1982)

Several tert-butyl percarbamates have been prepared by the reaction of amines with tert-butyl imidazoylpercarboxylate.The thermal decomposition of these peresters in solution led to the characteristic products of homolytic processes.The kinetic study of the thermolysis has been performed by Differential Scanning Microcalorimetry.It showed the influence of the nitrogen atom substitution on the percarbamate stability.The kinetic study of the decompositions of percarbamates derived from cyclic amines showed an important effect of the cycle size on the rate constant.Very different transition state levels are responsible for this phenomenon.A stereoelectronic origin-from the overlapping of the p-orbital of the nitrogen atom and the ? bond of the carboxyl- has been advanced to account for this result.

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