BOC-(S)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID

BOC-(S)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID - Names and Identifiers

Name	Boc-S-3-Amino-3-(2-bromo-phenyl)-propionic acid
Synonyms	Boc-b-Phe(2-Br)-OH Boc-L-3-Amino-3-(2-bromophenyl)-propionic acid Boc-S-3-Amino-3-(2-bromo-phenyl)-propionic acid BOC-(S)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID BOC-(S)-3-AMINO-3-(2-BROMO-PHENYL)-PROPANOIC ACID 3-aMino-3-(2-broMophenyl)-4-(tert-butoxy)-4-oxobutanoic acid (S)-3-(2-bromophenyl)-3-(tert-butoxycarbonylamino)propanoic acid (3S)-3-[(TERT-BUTOXY)CARBONYLAMINO]-3-(2-BROMOPHENYL)PROPANOIC ACID (betaS)-2-Bromo-beta-[[(1,1-dimethylethoxy)carbonyl]amino]benzenepropanoic acid
CAS	500770-75-2

BOC-(S)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID - Physico-chemical Properties

Molecular Formula	C14H18BrNO4
Molar Mass	344.2
Storage Condition	2-8°C

BOC-(S)-3-AMINO-3-(2-BROMO-PHENYL)-PROPIONIC ACID - Introduction

Boc-S-3-Amino-3-(2-bromo-phenyl)-propionic acid is an organic compound with the following properties:

1. Appearance: colorless to light yellow solid.
2. molecular formula: C13H16BrNO4S.
3. Molecular weight: 365.24g/mol.
4. melting point: about 75-80 degrees Celsius.
5. Solubility: Soluble in organic solvents (such as dimethyl sulfoxide and chloroform), insoluble in water.
6. storage conditions: should be stored in low temperature, dry, dark place.

Boc-S-3-Amino-3-(2-bromo-phenyl)-propionic acid has a variety of uses in chemical research and pharmaceuticals, including:

1. peptide synthesis: as a protective group, can be used for the synthesis of peptides and proteins.
2. drug synthesis: can be used as drug intermediates, involved in the synthesis of anti-tumor drugs, antiviral drugs.
3. biochemical research: for the synthesis of functional chemical peptides.
4. chemical analysis: to detect and analyze certain compounds, drugs or related molecules in biological samples.

The preparation method of Boc-S-3-Amino-3-(2-bromo-phenyl)-propionic acid can adopt the following steps:

1.3-amino -3-(2-bromophenyl) propionic acid is reacted with Boc ester, and esterification reaction is carried out under alkaline conditions.
2. by acid treatment, the Boc protecting group is removed from the reaction product to generate the final product Boc-S-3-amino -3-(2-bromophenyl) propionic acid.

The following safety information should be noted when using and handling Boc-S-3-amino -3-(2-bromophenyl) propionic acid:

1. Avoid contact with skin and eyes. If touched, flush the affected area with plenty of water and seek medical attention immediately.
2. Wear appropriate personal protective equipment during operation, including chemical protective gloves, goggles and protective clothing.
3. Use in a well-ventilated laboratory environment and avoid inhalation or ingestion of substances.
4. according to the chemical laboratory standard operating procedures for storage and handling.

Last Update：2024-04-09 02:00:49