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1,2-Ethanediamine, N-(2-phenoxyethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57404-41-8

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57404-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57404-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,0 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57404-41:
(7*5)+(6*7)+(5*4)+(4*0)+(3*4)+(2*4)+(1*1)=118
118 % 10 = 8
So 57404-41-8 is a valid CAS Registry Number.

57404-41-8SDS

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'-(2-phenoxyethyl)ethane-1,2-diamine

1.2 Other means of identification

Product number -
Other names -

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:57404-41-8 SDS

57404-41-8Relevant academic research and scientific papers

Tetrahydrofolate coenzyme models: Imidazolines as nucleophilic C1-transfer reagents

Jones,Nichols

, p. 1767 - 1770 (1990)

1-Benzyl-2-imidazoline is deprotonated at C-2 and alkylated by a sulphenylation-substitution sequence (to complete a formal C1-transfer), whereas arylation occurs by an unusual sulphenylation-sulphide contraction pathway.

ALPHA HYDROXY AMIDES

-

Page/Page column 37; 67; 68, (2014/04/17)

The present invention relates to alpha hydroxy amides including compounds of formula (I) and related compounds and their use in the prophylaxis and treatment of inflammatory disorders and diseases, wherein T1, T2, W and Rw has the meaning given in claim 1.

Coenzyme-inspired chemistry 1: The C-2 alkylation of 4,5-dihydroimidazoles

Jones, Raymond C.F.,Nichols, John R.

, p. 4114 - 4119 (2013/06/27)

Alkylation of 4,5-dihydroimidazoles at C-2 is accomplished using a double umpolung of the reactivity of that position, via sulfenylation of a nucleophilic C-2 lithio-species and substitution using an alkyl nucleophile. Arylation via unexpected sulfide con

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