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598-42-5

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598-42-5 Usage

Uses

Glycolamide may be used in the preparation of phosphoglycolamide.

General Description

Glycolamide, an isomer of glycine, can be synthesized by the ammonolysis of ethyl glycolate. The conformational analysis of glycolamide has been reported. Its diffusion coefficient in water and partial molal isothermal compressibility has been determined. Its thermodynamic properties have been investigated. Its osmotic and activity coefficients have been obtained.

Check Digit Verification of cas no

The CAS Registry Mumber 598-42-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 8 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 598-42:
(5*5)+(4*9)+(3*8)+(2*4)+(1*2)=95
95 % 10 = 5
So 598-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C2H5NO2/c3-2(5)1-4/h4H,1H2,(H2,3,5)

598-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxyacetamide

1.2 Other means of identification

Product number -
Other names Acetamide,2-hydroxy

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:598-42-5 SDS

598-42-5Relevant articles and documents

Micheel,Jung

, p. 1291 (1933)

Synthesis of α-amino and α-hydroxy acids under volcanic conditions: implications for the origin of life

Huber, Claudia,Eisenreich, Wolfgang,W?chtersh?user, Günter

scheme or table, p. 1069 - 1071 (2010/04/05)

Facile synthesis of α-hydroxy and α-amino acids is observed at temperatures from 145 to 280 °C with catalytic Ni2+, with cyano ligands as source for C and N, and with CO as a reductant and as a source for C. Implications for the problem of the origin of life are discussed.

HYDRATION OF CYANOHYDRINS IN WEEKLY ALKALINE SOLUTIONS OF BORIC ACID SALTS

Jammot, Jacqueline,Pascal, Robert,Commeyras, Auguste

, p. 563 - 564 (2007/10/02)

α-Hydroxyamides and α-hydroxyacids were prepared in satisfactory yield by heating aldehyde-derived cyanohydrins in aqueous solution in the presence of borax or alkaline borates.

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