RARECHEM AL CF 0887

RARECHEM AL CF 0887 - Names and Identifiers

Name	(S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID
Synonyms	Z-HOMOPHE-OH Z-HOMOPHENYLALANINE RARECHEM AL CF 0887 CBZ-L-HOMOPHENYL-ALA (S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID CBZ-(S)-2-AMINO-4-PHENYLBUTYRIC ACID N-ALPHA-CARBOBENZOXY-L-HOMOPHENYLALANINE N-ALPHA-CARBOBENZOXY-(+)-ALPHA-AMINO-4-PHENYLBUTYRIC ACID
CAS	127862-89-9

RARECHEM AL CF 0887 - Physico-chemical Properties

Molecular Formula	C18H19NO4
Molar Mass	313.35
Density	1.222±0.06 g/cm3(Predicted)
Boling Point	521.2±50.0 °C(Predicted)
BRN	3217335
pKa	3.93±0.10(Predicted)
Storage Condition	Sealed in dry,2-8°C

RARECHEM AL CF 0887 - Risk and Safety

WGK Germany

RARECHEM AL CF 0887 - Introduction

(S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID, chemical name (S)-2-(Z-amino)-4-PHENYLBUTYRIC ACID, is an organic compound. The following is a description of its nature, use, formulation and safety information:

Nature:
-Appearance: Usually white crystal or crystalline powder.
-Solubility: Can be dissolved in anhydrous methanol, anhydrous ethanol and dimethyl sulfoxide.

Use:
- (S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID is a very important chiral amino ACID protecting group, which is commonly used in peptide synthesis in organic synthesis, especially in the field of drug research and development has a wide range of applications. It can be used to protect the amino (carboxyl) functional groups in natural amino acids in order to carry out specific chemical reactions, such as the synthesis of peptide chains or pharmaceutical intermediates.
-In addition,(S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID can also be used as a raw material for stereochemical reagents and chiral Analytical reagents.

Method:
-The general method for preparing (S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID is to obtain Z-phenylaminobutyric ACID by reacting styrene compound with bromoacetic ACID, hydrazide condensation with acetic anhydride and imidazole under basic conditions gives (S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID.

Safety Information:
- (S)-2-(Z-AMINO)-4-PHENYLBUTYRIC ACID generally has low toxicity, but as an organic compound, it is still necessary to pay attention to safe operation.
-When using, avoid contact with skin or inhalation of its dust. Recommend operate in well-ventilated laboratory conditions and wear appropriate personal protective equipment such as lab gloves, safety glasses and protective face masks.
-If ingestion, skin contact or inhalation causes discomfort, seek medical attention immediately.

Last Update：2024-04-09 20:52:54