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Benzeneacetic acid, a-[[[4-(dimethylamino)phenyl]methylene]amino]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

83466-69-7

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83466-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83466-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,6 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83466-69:
(7*8)+(6*3)+(5*4)+(4*6)+(3*6)+(2*6)+(1*9)=157
157 % 10 = 7
So 83466-69-7 is a valid CAS Registry Number.

83466-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-paradimethylaminobenzylidene phenylglycinate de methyle

1.2 Other means of identification

Product number -
Other names methyl N-p-dimethylaminobenzylidenephenylglycinate

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:83466-69-7 SDS

83466-69-7Relevant academic research and scientific papers

X=Y-ZH Systems as Potential 1,3-Dipoles. Part 1. Background and Scope

Grigg, Ronald,Gunaratne, H. Q. Nimal,Kemp, James

, p. 41 - 46 (2007/10/02)

X=Y-ZH Systems are considered in general terms and divided into four classes according to the number of constituent atoms that possess lone-pair electrons.Those systems in which the central Y atom possesses a lone pair are shown to be capable of participa

Derecemization par protonation enantioselective. Application a un α-aminoacide, la phenylglycine

Duhamel, Lucette,Plaquevent, Jean-Christophe

, p. 75 - 83 (2007/10/02)

This work describes the application of deracemization by enantioselective protonation to α-aminoacid derivatives.Esters of phenylglycine are readly converted into Schiff bases.Melanation of the latter by a lithium amide, followed by protonation by a chiral acid, leads to the optically active starting materials (e.e. as high as 70percent).Chiral acids can easily be retrieved after protonation with excellent yields and conservation of enantiomeric purity.A mechanism responsible for the asymmetric induction is suggested by means of a study of the parameters modifying the selectivity, such as the nature of protecting groups, chiral acid, and lithium amide.

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