99295-78-0

Basic information

• Product Name: 3-Bromo-D-phenylalanine
• Synonyms: 3-Bromo-D-phenylalanine
• CAS NO: 99295-78-0
• Molecular Formula: C9H10BrNO2
• Molecular Weight: 244.09
• Product Categories: Amino Acids
• Mol File: 99295-78-0.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 368.4 °C at 760 mmHg
• Flash Point: 176.6 °C
• Appearance: /
• Density: 1.588 g/cm³
• Storage Temp.: Store at RT.
• PKA: 2.16±0.10(Predicted)
• CAS DataBase Reference: 3-Bromo-D-phenylalanine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Bromo-D-phenylalanine(99295-78-0)
• EPA Substance Registry System: 3-Bromo-D-phenylalanine(99295-78-0)

Safety Data

• Hazardous Substances Data: 99295-78-0(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 99295-78-0 differently. You can refer to the following data:
1. 3-Bromo-D-phenylalanine, can be used in the synthesis of various chemical compounds, such as 3-(Methylsulfonyl)-D-phenylalanine Hydrochloride, which has been found to be a potent LFA-1/ICAM-1 Antagonist SAR 1118 as an Ophthalmic Solution for treating dry eye.
2. 3-Bromo-D-phenylalanine, can be used in the synthesis of various chemical compounds, such as 3-(Methylsulfonyl)-D-phenylalanine Hydrochloride (M326188), which has been found to be a potent LFA-1/ICAM-1 Antagonist SAR 1118 as an Ophthalmic Solution for treating dry eye.

Chemical Properties

White powder

Upstream product

• 30163-20-3 2-amino-3-(3-bromophenyl)propanoic acid 
• 14473-91-7 3-bromocinnamic acid 
• 117391-50-1 3-amino-3-(3-bromo-phenyl)-propionic acid 
• 3132-99-8 m-bromobenzoic aldehyde 
• 14473-91-7 3-Bromocinnamic acid 
• 82278-73-7 (2S)-3-(3-bromophenyl)-2-[(tert-butoxycarbonyl)amino]propanoic acid 
• 823-78-9 meta-bromobenzyl bromide 
• 15017-44-4 diethyl (acetylamino)<(3-bromophenyl)methyl>propanedioate 

Relevant articles and documents

A novel phenylalanine ammonia-lyase from Pseudozyma antarctica for stereoselective biotransformations of unnatural amino acids

A novel phenylalanine ammonia-lyase of the psychrophilic yeast Pseudozyma antarctica (PzaPAL) was identified by screening microbial genomes against known PAL sequences. PzaPAL has a significantly different substrate binding pocket with an extended loop (26 aa long) connected to the aromatic ring binding region of the active site as compared to the known PALs from eukaryotes. The general properties of recombinant PzaPAL expressed in E. coli were characterized including kinetic features of this novel PAL with L-phenylalanine (S)-1a and further racemic substituted phenylalanines rac-1b-g,k. In most cases, PzaPAL revealed significantly higher turnover numbers than the PAL from Petroselinum crispum (PcPAL). Finally, the biocatalytic performance of PzaPAL and PcPAL was compared in the kinetic resolutions of racemic phenylalanine derivatives (rac-1a-s) by enzymatic ammonia elimination and also in the enantiotope selective ammonia addition reactions to cinnamic acid derivatives (2a-s). The enantiotope selectivity of PzaPAL with o-, m-, p-fluoro-, o-, p-chloro- and o-, m-bromo-substituted cinnamic acids proved to be higher than that of PcPAL.

Organocatalytic Enantioselective Addition of α-Aminoalkyl Radicals to Isoquinolines

With a dual organocatalytic system involving a chiral phosphoric acid and a dicyanopyrazine-derived chromophore (DPZ) photosensitizer and under the irradiation with visible light, an enantioselective Minisci-type addition of α-amino acid-derived redox-active esters (RAEs) to isoquinolines has been developed. A variety of prochiral α-aminoalkyl radicals generated from RAEs were successfully introduced on isoquinolines, providing a range of valuable α-isoquinoline-substituted chiral secondary amines in high yields with good to excellent enantioselectivities.

Second-order asymmetric transformation and its application for the practical synthesis of α-amino acids

We report a discovery of a new rimantadine [1-(1-adamantyl)ethanamine]-derived chiral ligand and its application for the preparation of α-amino acids using the second-order asymmetric transformation approach. The operational ease of experimental procedures coupled with excellent chemical yields and stereochemical outcome suggests some potential synthetic generality of this approach.