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Benzenamine, N-[[(1,1-dimethylethyl)dioxy]methyl]-N-ethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64254-25-7

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64254-25-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64254-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,2,5 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64254-25:
(7*6)+(6*4)+(5*2)+(4*5)+(3*4)+(2*2)+(1*5)=117
117 % 10 = 7
So 64254-25-7 is a valid CAS Registry Number.

64254-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(tert-butylperoxymethyl)-N-ethylaniline

1.2 Other means of identification

Product number -
Other names N-t-Butyldioxymethyl-N-ethylaniline

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:64254-25-7 SDS

64254-25-7Downstream Products

64254-25-7Relevant academic research and scientific papers

Oxidation of amines with hyper valent Tert-butylperoxyiodanes: Synthesis of imines and Tert-butylperoxyamino acetalsh

Ochiai, Masahito,Kajishima, Daisuke,Sueda, Takuya

, p. 71 - 76 (2007/10/03)

Reaction of secondary amines with 1-tert-butylperoxy-1,2-benziodoxol-3(1H)-one (2) undergoes dehydrogenation to afford imines in the presence of K2CO3, while oxidation of tertiary amines without base produces tert-butylperoxyamino acetals.

Amine Peroxides as Potential Antimalarials

Vennerstrom, Jonathan L.

, p. 64 - 67 (2007/10/02)

Six model amine peroxides (4-9) were synthesized as targeted antimalarial oxidants.They were approximately 1 order of magnitude more potent than tert-butyl hydroperoxide (3) in vitro against Plasmodium falciparum, but like 3, they were inactive in vivo against Plasmodium berghei.

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