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19391-83-4

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19391-83-4 Usage

General Description

A:B-diaminopropionic acid hydrochloride is a chemical compound that is a derivative of the amino acid beta-alanine. It is an organic compound with two amino groups, making it a diamine. As a hydrochloride salt, it is a crystalline solid that is highly soluble in water. It is used in the synthesis of peptides and other organic compounds, and it has potential applications in pharmaceutical research, particularly in the development of drugs that target neurological disorders and cancer. Its unique structure and properties make it a valuable building block for various chemical and biological applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19391-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,9 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19391-83:
(7*1)+(6*9)+(5*3)+(4*9)+(3*1)+(2*8)+(1*3)=134
134 % 10 = 4
So 19391-83-4 is a valid CAS Registry Number.

19391-83-4SDS

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 (+-)-2,4-diamino-butyric acid, monohydrochloride

1.2 Other means of identification

Product number -
Other names hydrochloride

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:19391-83-4 SDS

19391-83-4Relevant articles and documents

Preparation of enantiopure 2-acylazetidines and their reactions with chloroformates

Ma, Sang-ho,Yoon, Doo Ha,Ha, Hyun-Joon,Lee, Won Koo

, p. 269 - 271 (2007/10/03)

Enantiopure 1-phenylethylazetidine-2-carboxylates and 2-acylazetidines were prepared and reacted with chloroformates to yield α-chloro-γ-amino butyric acid esters and ketones from ring opening reaction of azetidinium ion intermediate in a completely regio- and stereoselective manner.

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