BOC-(R)-3-AMINO-3-(4-BROMO-PHENYL)-PROPANOIC ACID

BOC-(R)-3-AMINO-3-(4-BROMO-PHENYL)-PROPANOIC ACID - Names and Identifiers

Name	Boc-R-3-Amino-3-(4-bromo-phenyl)-propionic acid
Synonyms	BOC-PHG(4-BR)-(C*CH2)OH BOC-D-BETA-PHE(4-BR)-OH BOC-4-BROMO-L-BETA-PHENYLALANINE Boc-4-Bromo-L-beta-phenylalanine BOC-(R)-4-BETA-BROMOPHENYLALANINE BOC PROTECTED (R)-B-(P-BROMOPHENYL)-B-ALANINE Boc-R-3-Amino-3-(4-bromo-phenyl)-propionic acid BOC-(R)-3-AMINO-3-(4-BROMO-PHENYL)-PROPANOIC ACID BOC-(R)-3-AMINO-3-(4-BROMO-PHENYL)-PROPIONIC ACID N-BETA-T-BUTOXYCARBONYL-BETA-L-HOMO(4-BROMOPHENYL)GLYCINE
CAS	261380-20-5

BOC-(R)-3-AMINO-3-(4-BROMO-PHENYL)-PROPANOIC ACID - Physico-chemical Properties

Molecular Formula	C14H18BrNO4
Molar Mass	344.2
Density	1.5311 (rough estimate)
Melting Point	142.1 °C
Boling Point	479.1±40.0 °C(Predicted)
Appearance	Powder
Color	White
pKa	4.27±0.10(Predicted)
Storage Condition	2-8°C
Refractive Index	1.6500 (estimate)

BOC-(R)-3-AMINO-3-(4-BROMO-PHENYL)-PROPANOIC ACID - Risk and Safety

Safety Description	24/25 - Avoid contact with skin and eyes.
WGK Germany	3
HS Code	29242990

BOC-(R)-3-AMINO-3-(4-BROMO-PHENYL)-PROPANOIC ACID - Introduction

Boc-R-3-Amino-3-(4-bromo-phenyl)-propionic acid is an organic compound having the chemical formula Boc-R-C6H4BrCOOH wherein Boc represents a bis (methylpropoxy) carbonyl group and R represents a substituent.

Nature:
Boc-R-3-Amino -3-(4-bromophenyl) propionic acid is a solid and can exist stably at room temperature. It is soluble in some common organic solvents such as dimethyl sulfoxide (DMSO), dichloromethane and methanol.

Use:
Boc-R-3-amino -3-(4-bromophenyl) propionic acid is often used as an important intermediate in organic synthesis. It can be used to synthesize polypeptides, proteins, and other biologically active compounds. The compounds may also find application in the field of pharmaceutical research and development.

Preparation Method:
The preparation method of Boc-R-3-amino -3-(4-bromophenyl) propionic acid is generally carried out by an organic synthesis method. A common synthetic route involves the reaction of 3-amino -3-(4-bromophenyl) propionic acid with a Boc protecting group and appropriate purification steps to give the desired product.

Safety Information:
During handling and storage, care should be taken to avoid contact of the compound with skin, eyes and mucous membranes. It should be operated in a well-ventilated area and follow relevant laboratory safety procedures. For detailed safety information, refer to the relevant Safety Data Sheet (SDS).

Last Update：2024-04-09 02:00:49