848188-26-1

Basic information

• Product Name: L-4-Bromophenylglycine
• Synonyms: L-4-Bromophenylglycine;L-4-Br-Phg-OH;(S)-2-AMino-2-(4-broMophenyl)acetic acid
• CAS NO: 848188-26-1
• Molecular Formula: C₈H₈BrNO₂
• Molecular Weight: 230.05862
• Mol File: 848188-26-1.mol

Chemical Properties

• Boiling Point: 363.2±32.0 °C(Predicted)
• Appearance: /
• Density: 1.673±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 1.81±0.10(Predicted)
• CAS DataBase Reference: L-4-Bromophenylglycine(CAS DataBase Reference)
• NIST Chemistry Reference: L-4-Bromophenylglycine(848188-26-1)
• EPA Substance Registry System: L-4-Bromophenylglycine(848188-26-1)

Safety Data

• Hazardous Substances Data: 848188-26-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
L-4-Bromophenylglycine is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs and therapeutic agents. Its role in the creation of chiral ligands and catalysts is particularly significant in the production of enantiomerically pure compounds, which are essential for the efficacy and safety of many medications.
Used in Agrochemical Industry:
In the agrochemical sector, L-4-Bromophenylglycine is utilized as an intermediate in the synthesis of agrochemicals, playing a crucial role in the development of pesticides and other agricultural chemicals. Its contribution to the synthesis process helps in creating more effective and targeted agrochemicals to protect crops and enhance agricultural productivity.
Used in Chemical Research:
L-4-Bromophenylglycine is also used as a chiral building block in chemical research for the preparation of chiral ligands and catalysts. Its presence in these compounds is vital for facilitating asymmetric reactions, which are fundamental in the synthesis of enantiomerically pure compounds, crucial for various applications in the chemical and pharmaceutical industries.

Upstream product

• 67-66-3 chloroform 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 1228570-47-5 C₁₃H₁₆BrNO₄ 

Relevant articles and documents

ASYMMETRIC INDUCTIVE SYNTHESIS OF α-AMINOARYLACETIC ACIDS IN CHIRAL MICELLAR SYSTEM

In the micellar solution of chiral surfactant N-hexadecyl-N-methylephedrine bromide, seven α-aminoarylacetic acids were synthesized from corresponding aldehydes, the e.e.percent being about 28percent.