178933-04-5

178933-04-5 - Names and Identifiers

Name	(S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride
Synonyms	H-ALA(4-PYRI)-OH L-4-PYRIDYLALANINE H-ALA(4-PYRIDYL)-OH RARECHEM BK PT 0239 H-ALA(4'-PYRIDYL)-OH 3-(4-PYRIDYL)-ALANINE 3-(4-Pyridyl)-alanine.2HCl (S)-2-AMINO-3-(4-PYRIDYL)PROPIONIC ACID (S)-2-AMINO-3-(4'-PYRIDYL)PROPANOIC ACID (S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride
CAS	178933-04-5

178933-04-5 - Physico-chemical Properties

Molecular Formula	C8H10N2O2
Molar Mass	166.18
Melting Point	206 °C(dec.)
Storage Condition	Inert atmosphere,Room Temperature

178933-04-5 - Risk and Safety

WGK Germany

178933-04-5 - Introduction

(S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydroxychloride is an organic compound with the chemical name ((S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride). The following is a description of the properties, uses, preparation and safety information of the compound:

Nature:
-Appearance:(S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydroxychloride is a colorless crystalline or crystalline powder solid.
-Solubility: high solubility in water, soluble in alcohol and ether.
-Chemical properties: It is an amino acid hydrochloride with a lactone structure. It is a chiral compound and only exists in the L-configuration.

Use:
(S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride has important applications in biochemistry, medicinal chemistry and organic synthesis:
-Biological activity Research: It is an important amino acid derivative that can be used to study protein structure, enzyme-catalyzed reactions and interactions between biomolecules.
-Drug development: The compound can be used as an intermediate for the synthesis of drugs, for the synthesis of biologically active compounds, such as anti-cancer drugs, antiviral drugs and antidepressants.
-other applications:(S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride can also be used in organic synthesis catalyst, ligand or enzyme reaction research.

Method:
The preparation method of (S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride usually involves the following steps:
1. Add pyridine to the reaction vessel, and then add the appropriate amount of cyanoacetate.
2. L-Alanine Ester salt was added and the corresponding intermediate was generated.
3. The intermediate reacts with hydrochloric acid to generate (S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride.
4. By crystallization or centrifugation and other methods to obtain pure products.

Safety Information:
(S)-2-amino-3-(pyridin-4-yl)propanoic acid dihydrochloride is not currently classified as a substance of particular hazard. However, the safe use and handling of chemicals should follow general laboratory safety practices, including wearing appropriate protective measures, avoiding contact with skin and eyes, and observing correct handling and storage methods. Before use, it is recommended to read and observe the relevant safety data sheets and operating manuals.

Last Update：2024-04-09 20:45:29

Suzhou Haofan biological Co., Ltd.

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