AHPA,(2S,3R)-2-羟基-3-氨基-4-苯基丁酸AHPA

AHPA,(2S,3R)-2-羟基-3-氨基-4-苯基丁酸AHPA - Names and Identifiers

Name	3-AMINO-2-HYDROXY-4-PHENYLBUTYRIC ACID
Synonyms	AHPA 3-AMINO-2-HYDROXY-4-PHENYLBUTYRIC ACID 3-Amino-2-hydroxy-4-phenylbutanoic acid beta-Amino-alpha-hydroxybenzenebutanoic acid (2S,3R)-3-Amino-2-hydroxy-4-phenylbutyric acid (2S,3R)-3-Amino-2-hydroxy-4-phenylbutanoic acid (2S,3R)-3-amino-2-hydroxy-4-phenylbutanoic acid benzenebutanoic acid, beta-amino-alpha-hydroxy- Benzenebutanoic acid, b-amino-a-hydroxy-, (aS,bR)- Benzenebutanoic acid, β-?amino-?α-?hydroxy-?, (αS,?βR)?- Benzenebutanoic acid, beta-amino-alpha-hydroxy-, (R,S)-
CAS	59554-14-2
EINECS	1308068-626-2
InChI	InChI=1/C10H13NO3/c11-8(9(12)10(13)14)6-7-4-2-1-3-5-7/h1-5,8-9,12H,6,11H2,(H,13,14)/t8-,9+/m1/s1

AHPA,(2S,3R)-2-羟基-3-氨基-4-苯基丁酸AHPA - Physico-chemical Properties

Molecular Formula	C10H13NO3
Molar Mass	195.22
Density	1.285±0.06 g/cm3(Predicted)
Melting Point	235-237 °C (decomp)
Boling Point	428.5±45.0 °C(Predicted)
Flash Point	212.961°C
Vapor Presure	0mmHg at 25°C
pKa	2.97±0.17(Predicted)
Storage Condition	2-8°C
Refractive Index	1.595
Use	Ubenimex Intermediate

AHPA,(2S,3R)-2-羟基-3-氨基-4-苯基丁酸AHPA - Reference

Reference

1. Lian Xu, Li-Chao Wang, Bing-Mei Su, Xin-Qi Xu, Juan Lin, Multi-enzyme cascade for improving β-hydroxy-α-amino acids production by engineering L-threonine transaldolase and combining acetaldehyde elimination system, Bioresource Technology, Volume 310, 2020,

AHPA,(2S,3R)-2-羟基-3-氨基-4-苯基丁酸AHPA - Introduction

ACID is a chiral molecule with the chemical formula C10H13NO3.

Nature:
The ACID is a white crystalline solid that is soluble in water. It is an amino acid derivative with one amino group and one hydroxyl group. This compound usually exists in ionic form under physiological conditions because it has two ionized functional groups, amino and carboxyl.

Use:
The compound is commonly used as an intermediate in organic synthesis. It is a precursor of some important drugs in the field of drug synthesis. In addition, arbon ACID can also be used as a tool in the synthesis of certain chemical reagents and ligands, as well as in certain biological studies.

Preparation Method:
The ACID is usually obtained by chemical synthesis. A common preparation method is to use a simplified peptide synthesis reaction to synthesize the corresponding amino acid. By selective protection and deprotection reactions, the desired chiral molecule is obtained.

Safety Information:

Last Update：2024-04-09 20:52:54