(S)-3-AMINO-4-M-TOLYLBUTANOIC ACID

(S)-3-AMINO-4-M-TOLYLBUTANOIC ACID - Names and Identifiers

Name	(S)-3-Amino-4-(3-methyl-phenyl)-butyric acid-HCl
Synonyms	H-b-HoPhe(3-Me)-OH·HCl H-β-HoPhe(3-Me)-OH.HCl H-PHE(3-ME)-(C*CH2)OH HCL H-BETA-HOPHE(3-ME)-OH HCL (S)-3-AMINO-4-M-TOLYLBUTANOIC ACID (S)-3-Amino-4-(3-methyl-phenyl)-butyricacidCl 3-METHYL-L-BETA-HOMOPHENYLALANINE HYDROCHLORIDE L-BETA-HOMO(3-METHYLPHENYL)ALANINE HYDROCHLORIDE (S)-3-Amino-4-(3-methyl-phenyl)-butyric acid-HCl
CAS	270062-92-5

(S)-3-AMINO-4-M-TOLYLBUTANOIC ACID - Physico-chemical Properties

Molecular Formula	C11H15NO2
Molar Mass	193.24
Density	1.135±0.06 g/cm3(Predicted)
Boling Point	344.6±30.0 °C(Predicted)
pKa	3.81±0.10(Predicted)
Storage Condition	Room Temprature

(S)-3-AMINO-4-M-TOLYLBUTANOIC ACID - Introduction

(S)-3-Amino-4-(3-methyl-phenyl)-butyric acid-HCl is an organic compound also known as (S)-3-Amino-4-(3-methyl-phenyl)-butyric acid hydrochloride.

Properties of this compound:
-Appearance: White or off-white crystalline or powdery solid.
-Solubility: Soluble in water, slightly soluble in ethanol and chloroform.

Use of this compound:
-Pharmaceutical field: It can be used as a drug intermediate for the synthesis of drugs, especially antidepressants and anti-anxiety drugs.
-Research field: It can be used for the research of organic synthesis reactions and related research of chemical biology and drug discovery.

Preparation of this compound:
(S)-3-Amino-4-(3-methyl-phenyl)-butyric acid-HCl can be synthesized by the following steps:
1. (S)-3-amino -4-(3-methylphenyl) butyric acid reacts with hydrochloric acid to generate (S)-3-Amino-4-(3-methyl-phenyl)-butyric acid-HCl.

Safety information for this compound:
-harm to human body: may be irritating, contact with skin and eyes may cause irritation. Appropriate personal protective measures should be taken, such as wearing gloves, goggles and appropriate protective clothing.
-Storage and handling: should be stored in a dry, well-ventilated place, away from fire and oxidizing agents. Avoid contact with strong acids, strong bases and oxidants.

Last Update：2024-04-09 02:00:49