478183-65-2

Basic information

• Product Name: FMOC-D-PHE(2-I)-OH
• Synonyms: N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-2-IODO-D-PHENYLALANINE;FMOC-2-IODO-D-PHENYLALANINE;FMOC-D-PHE(2-I)-OH;(R)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(2-iodophenyl)propanoic acid;Fmoc-D-2-Iodophenylalanine;N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-iodo- D-Phenylalanine
• CAS NO: 478183-65-2
• Molecular Formula: C24H20INO4
• Molecular Weight: 513.32
• Product Categories: Amino Acid Derivatives
• Mol File: 478183-65-2.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: Store at 0°C
• CAS DataBase Reference: FMOC-D-PHE(2-I)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-D-PHE(2-I)-OH(478183-65-2)
• EPA Substance Registry System: FMOC-D-PHE(2-I)-OH(478183-65-2)

Safety Data

• Hazardous Substances Data: 478183-65-2(Hazardous Substances Data)

Usage

General Description

FMOC-D-PHE(2-I)-OH is a chemical compound consisting of a fluorenylmethoxycarbonyl (FMOC) protecting group attached to the amino group of the amino acid D-phenylalanine, which is further modified by the addition of an iodine atom at the 2-position. FMOC-D-PHE(2-I)-OH is commonly used in peptide synthesis as a building block for the creation of peptide chains. The FMOC protecting group is used to prevent unwanted reactions at the amino group, while the iodine atom can be used as a point of attachment for further modifications or for facilitating certain reactions. Overall, FMOC-D-PHE(2-I)-OH is an important component in the preparation of peptide-based drugs and biomolecules in various research and medical applications.