FMOC-D-PHE(2-F)-(C*CH2)OH - Names and Identifiers
FMOC-D-PHE(2-F)-(C*CH2)OH - Physico-chemical Properties
Molecular Formula | C25H22FNO4
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Molar Mass | 419.44 |
Storage Condition | 2-8°C |
FMOC-D-PHE(2-F)-(C*CH2)OH - Risk and Safety
FMOC-D-PHE(2-F)-(C*CH2)OH - Introduction
Boc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid is an organic compound with the chemical formula C20H19FNO4. It is a white to pale yellow solid powder.
Boc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid is often used as an amino acid protecting group in organic synthesis. It can be used to synthesize peptides and proteins, especially in solid phase synthesis. It is widely used in chemical synthesis to generate pharmacologically active polypeptides and protein structures. In addition, it is often used in the research and development of new drugs, biotechnology and chemical biology.
The preparation method of Boc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid is generally obtained by synthesis and purification of the compound. Specific synthetic routes and steps vary depending on the reactants, and commonly used methods include condensation reactions of carboxylic acids with amino acids and the introduction of protecting groups.
For safety information, Boc-(R)-3-Amino-4-(2-fluoro-phenyl)-butyric acid has low toxicity. As a chemical reagent, it should be handled in accordance with the general chemical practice. Wear appropriate protective equipment, such as lab gloves and goggles, to avoid direct contact with skin and eyes. It should be stored in a dry, well-ventilated place, away from fire and flammable materials.
This information is for reference only. Please follow the corresponding safety procedures when using or preparing the compound, and refer to the relevant literature and detailed information provided by the manufacturer.
Last Update:2024-04-10 22:29:15