1217610-39-3

Basic information

• Product Name: FMOC-D-4-CARBAMOYLPHE
• Synonyms: FMOC-D-4-CARBAMOYLPHE;FMOC-D-4-CARBAMOYLPHENYLALANINE;Fmoc-D-4-carbamoylphenylalanine≥ 99% (HPLC);(9H-Fluoren-9-yl)MethOxy]Carbonyl D-4-Carbamoylphe
• CAS NO: 1217610-39-3
• Molecular Formula: C25H22N2O5
• Molecular Weight: 430.45
• Product Categories: Phenylalanine analogs and other aromatic alpha amino acids
• Mol File: 1217610-39-3.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 713.4±60.0 °C(Predicted)
• Appearance: /
• Density: 1.336±0.06 g/cm3(Predicted)
• PKA: 3.69±0.10(Predicted)
• CAS DataBase Reference: FMOC-D-4-CARBAMOYLPHE(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-D-4-CARBAMOYLPHE(1217610-39-3)
• EPA Substance Registry System: FMOC-D-4-CARBAMOYLPHE(1217610-39-3)

Safety Data

• Hazardous Substances Data: 1217610-39-3(Hazardous Substances Data)

Usage

Description

FMOC-D-4-CARBAMOYLPHE, also known as Fmoc-D-4-Carbamoylphenylalanine, is a synthetic derivative of the amino acid phenylalanine. It is characterized by the presence of a carbamoyl group at the 4-position and a 9-fluorenylmethoxycarbonyl (Fmoc) protecting group. FMOC-D-4-CARBAMOYLPHE is a white powder and is used in the synthesis of various biologically active peptides and pharmaceuticals.

Uses

Used in Pharmaceutical Industry:
FMOC-D-4-CARBAMOYLPHE is used as a building block in the synthesis of peptides and pharmaceuticals for various therapeutic applications. Its unique structure allows for the incorporation of specific functional groups and properties into the final product, enhancing its biological activity and efficacy.
Used in Anticancer Applications:
FMOC-D-4-CARBAMOYLPHE is used in the preparation of somatostatin receptor antagonists, which are employed as antidiabetic agents. These antagonists help regulate insulin secretion and glucose metabolism, providing a potential treatment option for diabetes management.
Used in Peptide Synthesis:
FMOC-D-4-CARBAMOYLPHE is used as a protected amino acid in the synthesis of peptides. The Fmoc protecting group allows for selective deprotection and coupling reactions during peptide assembly, facilitating the synthesis of complex peptide sequences with high purity and yield.