273730-59-9

Basic information

• Product Name: AC-P-BROMO-DL-PHE-OH
• Synonyms: N-ALPHA-ACETYL-P-BROMO-DL-PHENYLALANINE;AC-P-BROMO-DL-PHENYLALANINE;AC-P-BROMO-DL-PHE-OH;ACETYL-4-BROMO-DL-PHENYLALANINE;AC-DL-PHE(4-BR)-OH;(RS)-Ac-2-amino-3-(4-bromophenyl)propionic acid;Acetyl-4-bromo-DL-phenylalanine≥ 98% (HPLC);3-(4-bromophenyl)-2-acetamidopropanoic acid
• CAS NO: 273730-59-9
• Molecular Formula: C11H12BrNO3
• Molecular Weight: 286.12
• Mol File: 273730-59-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 507.4±45.0 °C(Predicted)
• Appearance: /
• Density: 1.514±0.06 g/cm3(Predicted)
• Storage Temp.: Store at 0-5°C
• PKA: 3.51±0.10(Predicted)
• CAS DataBase Reference: AC-P-BROMO-DL-PHE-OH(CAS DataBase Reference)
• NIST Chemistry Reference: AC-P-BROMO-DL-PHE-OH(273730-59-9)
• EPA Substance Registry System: AC-P-BROMO-DL-PHE-OH(273730-59-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 273730-59-9(Hazardous Substances Data)

Usage

General Description

AC-P-BROMO-DL-PHE-OH is a synthetic organic compound consisting of a protected form of the amino acid phenylalanine with a bromine substituent attached. The "AC" designation likely refers to the use of an acetyl group to protect the amino group of the phenylalanine, while "DL" indicates that the compound is a racemic mixture of both the D and L forms of the phenylalanine enantiomers. The bromine atom is added to the phenylalanine side chain, potentially for use in chemical synthesis or as a research tool. AC-P-BROMO-DL-PHE-OH may be used in peptide synthesis, drug development, or as a precursor in the production of other chemical compounds.

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 154192-52-6 C₁₁H₁₀BrNO₃ 
• 186605-19-6 4-(4-bromophenyl)methylene-2-methyl-5(4H)-oxazolone 
• 14091-15-7 p-bromo-DL-phenylalanine 
• 171095-12-8 N-acetyl-4-bromophenylalanine 
• 108-24-7 acetic anhydride 
• 1353886-56-2 ethyl 3-(4-bromophenyl)-2-(hydroxyimino)propionate 
• 140202-28-4 ethyl 4-bromo-N-acetylphenylalaninate 

Downstream Products

• 24250-84-8 H-p-BrPhe-OH 

Relevant articles and documents

Asymmetric synthesis of unnatural amino acids and tamsulosin chiral intermediate

An efficient and enantioselective hydrogenation of N-acetylamino phenyl acrylic acids was successfully developed by using ruthenium catalyst. This methodology is important in the field of pharmaceuticals and provides a new process for the preparation of unnatural amino acids and tamsulosin chiral intermediate.

Convenient method for reduction of C-N double bonds in oximes, imines, and hydrazones using sodium Borohydride-Raney ni system

(Chemical Equation Presented) A practical method has been developed for reduction of C-N double bond in oximes, imines, and hydrazones with sodium borohydride catalyzed by Raney Ni. The reactions were carried out in basic aqueous solution, and the desired products were obtained in moderate yields after a simple procedure. This method can be applied to synthesize simpler aliphatic or aromatic amines and its analogs. Copyright Taylor & Francis Group, LLC.

Novel atropisomeric bisphosphine ligands with a bridge across the 5,5′-position of the biphenyl for asymmetric catalysis

A new type of atropisomeric bisphosphine ligand 2 with a bridge across the 5,5′-position of the biphenyl has been developed. The axial chirality of this type of ligands can be retained by macrocyclic ring strain produced from 5,5′-linkage of the biphenyl