201485-38-3

Basic information

• Product Name: FMOC-D-HOCIT-OH
• Synonyms: (R)-2-FLUORENYLMETHOXYCARBONYLAMINO-6-UREIDOHEXANOIC ACID;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-D-HOMOCITRULLINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-D-HOMOCITRULLINE;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON-CARBAMOYL-D-LYSINE;N-ALPHA-FMOC-D-HOMOCITRULLINE;FMOC-N-EPSILON-CARBAMOYL-D-LYSINE;FMOC-D-LYS(CARBAMOYL)-OH;FMOC-D-LYS(CONH2)-OH
• CAS NO: 201485-38-3
• Molecular Formula: C22H25N3O5
• Molecular Weight: 411.45
• Mol File: 201485-38-3.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 676.0±55.0 °C(Predicted)
• Appearance: /
• Density: 1.292±0.06 g/cm3(Predicted)
• Storage Temp.: Store at RT.
• PKA: 3.89±0.21(Predicted)
• CAS DataBase Reference: FMOC-D-HOCIT-OH(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-D-HOCIT-OH(201485-38-3)
• EPA Substance Registry System: FMOC-D-HOCIT-OH(201485-38-3)

Safety Data

• Hazardous Substances Data: 201485-38-3(Hazardous Substances Data)

Usage

General Description

FMOC-D-HOCIT-OH is a chemical compound typically used in the field of biochemistry and molecular biology. It is a derivative of the amino acid aspartic acid and belongs to the family of FMOC-protected amino acids, which are often used in peptide synthesis. The FMOC group provides protection for the carboxyl group of the amino acid, allowing for controlled and stepwise synthesis of peptides. The addition of the HOCIT-OH moiety to the amino acid provides specific functionalization and modification, allowing for the incorporation of diverse properties into the resulting peptide. Overall, FMOC-D-HOCIT-OH plays a crucial role in the controlled synthesis of peptides with tailored properties for various applications.