4-Phenyl-DL-Phenylalanine

4-Phenyl-DL-Phenylalanine - Names and Identifiers

Name	2-amino-3-biphenyl-4-ylpropanoic acid (non-preferred name)
Synonyms	LogP DL-4-Phenyl-Phe-OH DL-BIPHENYLALANINE 4-Phenyl-DL-Phenylalanine 2-AMINO-3-BIPHENYL-4-YL-PROPIONIC ACID 2-Amino-3-(biphenyl-4-yl)propanoic acid 2-amino-3-(4-phenylphenyl)propanoic acid [1,1'-Biphenyl]-4-propanoicacid, a-aMino (RS)-2-AMINO-3-(4-BIPHENYL)PROPIONIC ACID DL-4-Phenyl-Phe-OH 4-Phenyl-DL-Phenylalanine 2-amino-3-biphenyl-4-ylpropanoic acid (non-preferred name) 2-Amino-3-(biphenyl-4-yl)propanoic acid (non-preferred name)
CAS	76985-08-5
InChI	InChI=1/C15H15NO2/c16-14(15(17)18)10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9,14H,10,16H2,(H,17,18)

4-Phenyl-DL-Phenylalanine - Physico-chemical Properties

Molecular Formula	C15H15NO2
Molar Mass	241.29
Density	1.19g/cm³
Boling Point	428.6°C at 760 mmHg
Flash Point	213°C
Vapor Presure	4.15E-08mmHg at 25°C
Storage Condition	Keep in dark place,Inert atmosphere,Room temperature
Refractive Index	1.607

4-Phenyl-DL-Phenylalanine - Introduction

A. acidula (non-preferred name) is an organic compound, also known as 2-amino-3-biphenylpropionic acid, with the chemical formula C15H15NO2.

Properties: acid (non-preferred name) is a colorless crystalline solid with optical isomers of phenylalanine, that is, it contains two isomers, levorotatory (L form) and dextrorotatory (D form). It has different solubility in different solvents and is soluble in hydrochloric acid, alcohols and water. It is relatively stable in a neutral environment, but will decompose under strong acid, strong alkali and high temperature conditions.

Uses: acid (non-preferred name) is mainly used in synthesis and biochemical research. It can be used as an intermediate in organic synthesis for the synthesis of drugs, dyes, optical materials and organic chemical reagents. In the field of biochemistry, it is often used to study amino acid metabolism and protein structure.

preparation method: preferred acid (non-name) has many preparation methods, and the commonly used methods include:

1. through the halogenated substitution reaction of phenylacetic acid: the first reaction of phenylacetic acid with halogenated reagents (such as brominated alkyl or chlorinated alkyl) to generate the corresponding halogenated phenylacetic acid. Then, the phenylacetic acid halide is reacted with aniline to give a phenyl acid (non-preferred name).

2. through the rearrangement reaction of the substrate: 2-biphenyl propionic acid is reacted with amino acid, and acid (non-preferred name) is obtained through acid-catalyzed rearrangement reaction.

Safety information: Limited data on the toxicity of preferred acid (non-name) to humans. As a chemical, it should follow general safety measures. Inhalation, ingestion and contact with skin should be avoided. When using, wear appropriate personal protective equipment to avoid contact with eyes and skin, and ensure that the operation is carried out in a well-ventilated place. If accidental contact or accidental ingestion occurs, seek medical attention.

Last Update：2024-04-09 02:00:48