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2-ethylperoxy-2-methyl-propane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20396-54-7

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20396-54-7 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 338, 1950 DOI: 10.1021/ja01157a089

Check Digit Verification of cas no

The CAS Registry Mumber 20396-54-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20396-54:
(7*2)+(6*0)+(5*3)+(4*9)+(3*6)+(2*5)+(1*4)=97
97 % 10 = 7
So 20396-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O2/c1-5-7-8-6(2,3)4/h5H2,1-4H3

20396-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylperoxy-2-methylpropane

1.2 Other means of identification

Product number -
Other names tert.-Butyl-ethyl-peroxid

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:20396-54-7 SDS

20396-54-7Relevant academic research and scientific papers

RATE CONSTANTS FOR THE FORMATION OF OXIRANES BY γ-SCISSION IN SECONDARY β-t-BUTYLPEROXYALKYL RADICALS

Bloodworth A. J.,Courtneidge, J. L.,Davies, Alwyn G.

, p. 523 - 528 (2007/10/02)

Rate constants for the title reactions have been determined from the ratios of oxirane to peroxide obtained in the reductons of β-bromoalkyl t-butyl peroxides with tributyltin hydride.At ca. 298 K the rate constants are 0.32, 1.12, 1.96, 2.0 and 6.2E6 s-1 for β-t-butylperoxy derivatives of trinorbornan-2-yl (exo) cyclohexyl, 1-methylpropyl , cyclopentyl and 1-ethylbutyl, respectively.The results are discussed in terms of steric and electronic effects in the transition state leading to ring closure of the radicals.

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