FMOC-PHE(4-ME)-(C*CH2)OH - Names and Identifiers
FMOC-PHE(4-ME)-(C*CH2)OH - Physico-chemical Properties
Molecular Formula | C26H25NO4
|
Molar Mass | 415.48 |
Storage Condition | 2-8°C |
FMOC-PHE(4-ME)-(C*CH2)OH - Risk and Safety
FMOC-PHE(4-ME)-(C*CH2)OH - Introduction
Fmoc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid is an amino acid derivative. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: White to light yellow solid.
-Molecular formula: C22H21NO3.
-Molecular weight: 347.41g/mol.
-Melting point: about 165-168°C.
-Solubility: Soluble in organic solvents such as dichloromethane, methanol, dimethylformamide, etc.
Use:
- Fmoc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid is a reagent commonly used in solid-phase synthesis and peptide synthesis as a protecting group for amino acids.
-It can be used for the synthesis of biologically active peptides, proteins and their analogs.
Preparation Method:
Fmoc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid can be prepared as follows:
1. First, butyric acid derivatives were synthesized through a series of chemical reactions.
2. Then, dimethylamino (N,N-dimethylamine) and an acid catalyst are added to the derivative.
3. Finally, Fmoc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid is generated through the reaction.
Safety Information:
- Fmoc-(S)-3-Amino-4-(4-methyl-phenyl)-butyric acid is relatively safe under correct operation.
-As a chemical substance, it is necessary to strictly follow laboratory safety procedures.
-Dust in direct contact with the skin, eyes or by inhalation of this compound may cause irritation and should be avoided.
-Appropriate protective equipment such as goggles, gloves and laboratory ventilation should be provided when using the compound.
Please note that due to the complexity and uncertainty of chemical properties, it is recommended to consult relevant chemical literature, safety data sheets and occupational safety guidelines before use to ensure correct handling and handling.
Last Update:2024-04-10 22:29:15