BOC-(S)-3-AMINO-4-(2-FLUORO-PHENYL)-BUTYRIC ACID

BOC-(S)-3-AMINO-4-(2-FLUORO-PHENYL)-BUTYRIC ACID - Names and Identifiers

Name	Boc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid
Synonyms	RARECHEM AK PT F069 FMOC-PHE(2-F)-(C*CH2)OH FMOC-BETA-HOPHE(2-F)-OH FMOC-2-FLUORO-L-BETA-HOMOPHENYLALANINE FMOC-(S)-3-AMINO-4-(2-FLUOROPHENYL)BUTANOIC ACID Boc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid FMOC-(S)-3-AMINO-4-(2-FLUORO-PHENYL)-BUTYRIC ACID N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(2-FLUOROPHENYL)ALANINE N-(9-FLUORENYLMETHOXYCARBONYL)-(S)-3-AMINO-4-(2-FLUOROPHENYL)BUTANOIC ACID
CAS	270596-49-1

BOC-(S)-3-AMINO-4-(2-FLUORO-PHENYL)-BUTYRIC ACID - Physico-chemical Properties

Molecular Formula	C25H22FNO4
Molar Mass	419.44
Storage Condition	2-8°C

BOC-(S)-3-AMINO-4-(2-FLUORO-PHENYL)-BUTYRIC ACID - Risk and Safety

Hazard Class

IRRITANT

BOC-(S)-3-AMINO-4-(2-FLUORO-PHENYL)-BUTYRIC ACID - Introduction

Boc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid is an organic compound having the chemical structural formula Fmoc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid.

Properties Boc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid is a white crystalline solid. It has the properties of an amino acid, contains a chiral center, and can exist in two enantiomers. It has a molecular weight of 341.34g/mol.

Boc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid is mainly used in organic synthesis as a raw material for the synthesis of peptides and proteins. It can be used to synthesize polypeptides by solid phase synthesis, wherein Fmoc represents a 9-fluoromethoxycarbonyl protecting group. The compounds can also be used to study the development of chiral catalysts and drug molecules.

In terms of preparation method, Boc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid can be obtained by condensation reaction of Fmoc amino acid with 2-fluorobenzoic acid. Selective protection of the chiral center is then required to give the (S)-isomer.

In terms of safety information, the handling of chemical substances should follow the laboratory's safety procedures. Since Boc-(S)-3-Amino-4-(2-fluoro-phenyl)-butyric acid is an organic compound, it may have irritation to skin, eyes and other tissues. During use, direct contact with the skin and inhalation of its dust should be avoided. If you come into contact with this compound, wash it immediately with plenty of water.

Last Update：2024-04-10 22:30:50