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

77290-59-6

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77290-59-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77290-59-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,9 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 77290-59:
(7*7)+(6*7)+(5*2)+(4*9)+(3*0)+(2*5)+(1*9)=156
156 % 10 = 6
So 77290-59-6 is a valid CAS Registry Number.

77290-59-6SDS

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 (4-nitro-benzoylamino)-phenyl-acetic acid ethyl ester

1.2 Other means of identification

Product number -
Other names α-(p-Nitrobenzoylamino)-phenylessigsaeureethylester

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:77290-59-6 SDS

77290-59-6Relevant academic research and scientific papers

Metalloporphyrin-promoted rearrangement of 2-alkyloxaziridines

Suda,Umehara,Hino

, p. 839 - 841 (2007/10/02)

Transformation of 2-alkyloxaziridines to the corresponding amides is efficiently catalyzed by high-valent metalloporphyrins. This novel rearrangement was used to create a peptide bond and the precursor of a dipeptide ''aspartame'' was obtained in good yield.

BASE PROMOTED OXIDATIVE DECARBOXYLATION OF ETHYL PHENYLGLYCINATE VIA OXAZIRIDINE

Yijima, Chino,Hino, Fumio,Suda, Kohji

, p. 4725 - 4726 (2007/10/02)

Base catalyzed decompositions of 2-(α-ethoxycarbonyl-benzyl)-3-phenyl-oxaziridines carried out in benzene in an atmosphere of oxygen yielded N-benzoyl benzamides along with ethyl phenylglyoxylate imine and benzaldehydes.

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