36097-42-4

Basic information

• Product Name: AC-P-AMINO-PHE-OME
• Synonyms: N-ALPHA-ACETYL-P-AMINO-L-PHENYLALANINE METHYL ESTER;AC-P-AMINO-PHENYLALANINE-OME;AC-P-AMINO-PHE-OME;AC-PHE(4-NH2)-OME;ACETYL-P-AMINO-L-PHE-OME;AC-4-AMINO-L-PHENYLALANINE METHYL ESTER;Ac-p-amino-phen-OMe;Ac-Phe(4-NH2)-OMe·HCl
• CAS NO: 36097-42-4
• Molecular Formula: C₁₂H₁₆N₂O₃
• Molecular Weight: 236.27
• Mol File: 36097-42-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 404.4 °C at 760 mmHg
• Flash Point: 198.4 °C
• Appearance: /
• Density: 1.203 g/cm³
• Storage Temp.: -15°C
• CAS DataBase Reference: AC-P-AMINO-PHE-OME(CAS DataBase Reference)
• NIST Chemistry Reference: AC-P-AMINO-PHE-OME(36097-42-4)
• EPA Substance Registry System: AC-P-AMINO-PHE-OME(36097-42-4)

Safety Data

• Hazardous Substances Data: 36097-42-4(Hazardous Substances Data)

Usage

General Description

AC-P-AMINO-PHE-OME is a chemical compound that belongs to the group of amino acid derivatives. It is composed of a peptide bond, an amino group, a phenyl group, and an omega functional group. AC-P-AMINO-PHE-OME is commonly used in organic synthesis and pharmaceutical research due to its potential biological activity and diverse chemical properties. It may exhibit unique pharmacological effects and is being investigated for its potential use in drug development. AC-P-AMINO-PHE-OME is of interest to researchers studying the structure-activity relationships of bioactive compounds and seeking to develop new molecules with therapeutic potential.

Upstream product

• 36097-39-9 (S)-methyl 2-acetamido-3-(4-nitrophenyl)propanoate 
• 3618-96-0 (S)-N-acetylphenylalanine 
• 17363-92-7 N-acetyl-4-nitro-L-phenylalanine 
• 7440-66-6 zinc 

Downstream Products

• 864238-42-6 D,L-4-Acetamido-N-acetyl-3-nitrophenylalanine methyl ester 
• 1184247-93-5 2-acetylamino-3-[4-(5-phenyl-tetrazol-2-yl)-phenyl]-propionic acid methyl ester 
• 186760-89-4 methyl (2S)-2-ethanamido-3-(4-methanamidophenyl)propanoate 
• 60521-91-7 Ac-Phe(4-NHAc)-OMe 

Relevant articles and documents

Pyridyl Radical Cation for C?H Amination of Arenes

Electron-transfer photocatalysis provides access to the elusive and unprecedented N-pyridyl radical cation from selected N-substituted pyridinium reagents. The resulting C(sp2)?H functionalization of (hetero)arenes furnishes versatile intermediates for the development of valuable aminated aryl scaffolds. Mechanistic studies that include the first spectroscopic evidence of a spin-trapped N-pyridyl radical adduct implicate SET-triggered, pseudo-mesolytic cleavage of the N?X pyridinium reagents mediated by visible light.

Method for preparing enantiomeric forms of amino alkylaminophenyl propanoic acid

A process for preparing an enantiomeric form of 2-amino-3-(4-alkylaminophenyl)-propanoic acid of formula (I) or a salt thereof: STR1 in which Alk represents an alkyl radical containing 1 to 2 carbon atoms, from (L)-phenylalanine to obtain the (S)-enantiomer of 2-amino-3-(4-alkylaminophenyl)-propanoic acid, or from (D)-phenylalanine to obtain the (R)-enantiomer of 2-amino-3-(4-alkylaminophenyl)propanoic acid.

Amino acids and esters thereof useful as antihypertensive agents

A compound of the formula STR1 possesses antihypertensive activity. Also provided are methods for the preparation of the compounds as well as pharmaceutical formulations and methods for their use as antihypertensive agents.