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Butanoic acid, 3-amino-4-(cyclohexylamino)-4-oxo-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30239-40-8

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30239-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30239-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,3 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30239-40:
(7*3)+(6*0)+(5*2)+(4*3)+(3*9)+(2*4)+(1*0)=78
78 % 10 = 8
So 30239-40-8 is a valid CAS Registry Number.

30239-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-amino-4-(cyclohexylamino)-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names Butanoic acid,3-amino-4-(cyclohexylamino)-4-oxo-,(S)

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:30239-40-8 SDS

30239-40-8Downstream Products

30239-40-8Relevant academic research and scientific papers

Studies on N-Glycopeptides. II. Separation of α- and β-Amide of N-(L-Aspartyl)-β-D-glucopyranosylamine Obtained via N-(Benzyloxycarbonyl)-L-aspartic Anhydride

Tamura, Masahiro,Nishizaki, Hiroshi,Miyazaki, Chiemi,Okai, Hideo

, p. 3167 - 3172 (2007/10/02)

A mixture of N-(L-α-aspartyl)- and N-(L-β-aspartyl)-β-D-glucopyranosylamine was obtained by the condensation of N-(benzyloxycarbonyl)-L-aspartic anhydride with β-D-glucopyranosylamine.Attempts to separate the mixture by using cation-exchange chromatography, a copper(II) complex, and fractional recrystallization were carried out.These separations gave good yields of the desired β-amine.

Determination of Enantiomers of Amino Acids by Reversed Phase High Performance Liquid Chromatography

Gilon, C.,Leshem, R.,Grushka, Eli

, p. 1206 - 1209 (2007/10/02)

The chromatographic resolution of enantiomeric amino acids is accomplished on reverse phase columns using aqueous mobile phases containing the chiral reagent L-aspartylcyclohexylamide-Cu(II).This reagent has the additional advantage that t

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