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102872-00-4

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102872-00-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102872-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,7 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102872-00:
(8*1)+(7*0)+(6*2)+(5*8)+(4*7)+(3*2)+(2*0)+(1*0)=94
94 % 10 = 4
So 102872-00-4 is a valid CAS Registry Number.

102872-00-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-benzamido-4-oxopentanoic acid

1.2 Other means of identification

Product number -
Other names 5-benzoylamino-4-oxo-valeric acid

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:102872-00-4 SDS

102872-00-4Relevant articles and documents

Preparation method of 5-aminolevulinic acid hydrochloride

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Paragraph 0028; 0035; 0038; 0040-0042; 0045, (2018/01/14)

The invention relates to a preparation method of 5-aminolevulinic acid hydrochloride, belonging to the technical field of drug intermediate synthesis. In order to solve the problems of long route and great pollution at present, the invention provides the preparation method of the 5-aminolevulinic acid hydrochloride. The preparation method is characterized in that the method comprise the following steps of under the existence of organic alkali and DMAP, enabling benzoyl glycine to react with butanedioic anhydride by using Dakin-West to obtain benzoyl aminolevulinic acid; under the existence of hydrochloric acid, enabling the benzoyl aminolevulinic acid to be subjected to hydrolysis reaction to obtain the 5-aminolevulinic acid hydrochloride. The synthetic method has the advantages that the reaction route is short, the raw materials are convenient to obtain, the cost is low, the reaction operation is simple and convenient and the pollution is less, and the method has the effects of high product yield and high purity.

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