201351-59-9

Basic information

• Product Name: AC-P-IODO-D-PHE-OH
• Synonyms: AC-D-PHE(4-I)-OH;ACETYL-4-IODO-D-PHENYLALANINE;AC-P-IODO-D-PHENYLALANINE;AC-P-IODO-D-PHE-OH;N-ALPHA-ACETYL-P-IODO-D-PHENYLALANINE;(R)-Ac-2-amino-3-(4-iodophenyl)propionic acid;Acetyl-4-iodo-D-phenylalanine≥ 97% (HPLC)
• CAS NO: 201351-59-9
• Molecular Formula: C11H12INO3
• Molecular Weight: 333.12
• Mol File: 201351-59-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 501.4 °C at 760 mmHg
• Flash Point: 257 °C
• Appearance: /
• Density: 1.71 g/cm³
• Storage Temp.: 2-8°C
• PKA: 3.52±0.10(Predicted)
• CAS DataBase Reference: AC-P-IODO-D-PHE-OH(CAS DataBase Reference)
• NIST Chemistry Reference: AC-P-IODO-D-PHE-OH(201351-59-9)
• EPA Substance Registry System: AC-P-IODO-D-PHE-OH(201351-59-9)

Safety Data

• Hazardous Substances Data: 201351-59-9(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 1991-81-7 p-iodophenylalanine 
• 108-24-7 acetic anhydride 
• 1991-81-7 4-iodo-L-phenylalanine 

Relevant articles and documents

Bio- And Medicinally Compatible α-Amino-Acid Modification via Merging Photoredox and N-Heterocyclic Carbene Catalysis

An N-heterocyclic carbene and photoredox cocatalyzed α-amino-acid decarboxylative carbonylation reaction is presented. This method displays good scope generality, providing a direct pathway to access various downstream α-amino ketones under bio- and medicinally compatible conditions. Moreover, this strategy is appealing to chemical biology because it has great potential for the chemical modification of peptides or the late-stage synthesis of keto-peptides.