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2-ACETOXY-N-(DIPHENYLMETHYLENE)GLYCINE ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97611-55-7

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97611-55-7 Usage

Chemical compound

2-ACETOXY-N-(DIPHENYLMETHYLENE)GLYCINE ETHYL ESTER

Health risks

may pose risks if inhaled or ingested, may cause skin and eye irritation
Handle with care

Check Digit Verification of cas no

The CAS Registry Mumber 97611-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,6,1 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 97611-55:
(7*9)+(6*7)+(5*6)+(4*1)+(3*1)+(2*5)+(1*5)=157
157 % 10 = 7
So 97611-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H19NO4/c1-3-23-19(22)18(24-14(2)21)20-17(15-10-6-4-7-11-15)16-12-8-5-9-13-16/h4-13,18H,3H2,1-2H3

97611-55-7SDS

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 ethyl 2-acetyloxy-2-(benzhydrylideneamino)acetate

1.2 Other means of identification

Product number -
Other names ethyl 2-acetoxy-2-diphenylmethyleneaminoacetate

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:97611-55-7 SDS

97611-55-7Relevant academic research and scientific papers

COMPOSITIONS AND METHODS USING THE SAME FOR TREATMENT OF NEURODEGENERATIVE AND MITOCHONDRIAL DISEASE

-

Page/Page column 124, (2015/09/22)

The present disclosure is directed, in part, to compounds, or pharmaceutically acceptable salts thereof, for the treatment and/or prevention of neurodegenerative disease and/or mitchonodrial disease including Parkinson's disease and Leigh's disease.

Anodic methoxylation and acetoxylation of imines and imidates

Baba, Daisuke,Fuchigami, Toshio

, p. 3133 - 3136 (2007/10/03)

Anodic oxidation of cyclic imidates, 2-aryl-2-oxazolines, in methanol provided the corresponding 4-methoxylated products. Anodic α-methoxylation and α-acetoxylation of open-chain imines derived from glycine esters and benzophenone were also achieved using a bromide ion mediator. On the other hand, anodic α-acetoxylation of CF3-containing imine and imidate was successful without use of the bromine mediator. This is the first example of successful anodic α-substitution of imines and imidates.

PREPARATION OF AN ELECTROPHILIC GLYCINE CATION EQUIVALENT AND ITS REACTION WITH HETEROATOM NUCLEOPHILES

O'Donnell, Martin J.,Bennett, William D.,Polt, Robin L.

, p. 695 - 698 (2007/10/02)

A variety of heteroatom substituted Schiff base amino esters 4-7 are prepared either from the benzophenone imine of glycine ethyl ester (3) or by reaction of acetate 4 with heteroatom nucleophiles.

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