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Glycine, N-formyl-N-(4-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90544-84-6

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90544-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90544-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,4 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90544-84:
(7*9)+(6*0)+(5*5)+(4*4)+(3*4)+(2*8)+(1*4)=136
136 % 10 = 6
So 90544-84-6 is a valid CAS Registry Number.

90544-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-formyl-N-(4-nitro-phenyl)-glycine

1.2 Other means of identification

Product number -
Other names N-Formyl-N-(4-nitro-phenyl)-glycin

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:90544-84-6 SDS

90544-84-6Relevant academic research and scientific papers

Microwave-assisted deformylation of N-aryl formamide by KF on basic Al2O3

Ge, Yiyu,Hu, Longqin

, p. 4585 - 4588 (2008/02/06)

The formyl group was successfully removed from N-aryl formamide by KF on a solid support of basic Al2O3 in 4-20 min with microwave irradiation. The conditions mimic base-catalyzed hydrolysis of formamide and are compatible with carbamates and t-butyl esters, but not methyl, ethyl, and benzyl esters.

Synthesis of Strombine. A New Method for Monocarboxymethylation of Primary Amines

Kihlberg, Jan,Bergman, Rolf,Wickberg, Boerje

, p. 911 - 916 (2007/10/02)

Many common methods for monocarboxymethylation of primary amines give various amounts of dialkylated by-products.In this work the reaction of two equivalents of glyoxilic acid with representative primary aliphatic and aromatic amines, as well as with amino acids and a dipeptide, is shown to give only the N-(carboxymethyl)-N-formyl derivative of the amine under mild conditions in carboxylic acid solvents.Hydrolysis then produces the monocarboxymethylated primary amine in good to exellent overall yield.Proof that the intermediate product is not obtained via the Leuckart reaction is given.

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