Benzenebutanoic acid, 3-bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βR)-
Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid
CAS:
Molecular Formula: C25H22BrNO4
Benzenebutanoic acid, 3-bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βR)- - Names and Identifiers
| Name | Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid |
| Synonyms | Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid Benzenebutanoic acid, 3-bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βR)- |
Benzenebutanoic acid, 3-bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βR)- - Physico-chemical Properties
| Molecular Formula | C25H22BrNO4 |
| Molar Mass | 480.35 |
| Density | 1.429±0.06 g/cm3(Predicted) |
| Boling Point | 673.0±55.0 °C(Predicted) |
| pKa | 4.37±0.10(Predicted) |
| Storage Condition | 2-8°C |
Benzenebutanoic acid, 3-bromo-β-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-, (βR)- - Introduction
Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid is an organic compound with the chemical formula C25H20BrNO4. It is white or off-white in nature and soluble in common organic solvents such as dimethyl sulfoxide and dimethylformamide.
Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid is commonly used in peptide synthesis reactions in solid phase synthesis. It is introduced as a protective group on the side chain of the amino acid to control the synthesis process and the selectivity of the product.
the method for preparing Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid generally adopts a chemical synthesis method, which can be obtained by reacting (R)-3-amino -4-(3-bromophenyl) butyric acid with Fmoc-Cl. Specific operating conditions need to refer to the relevant literature or experimental methods.
Regarding safety information, avoid direct contact with skin, eyes or inhalation of dust during operation. Operate in a well-ventilated laboratory environment and take appropriate personal protective measures, such as wearing protective gloves and goggles. During use or storage, keep the container sealed and avoid high temperature and fire sources. For more detailed recommendations on safe handling and handling, refer to the relevant dangerous goods instructions or contact a professional.
Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid is commonly used in peptide synthesis reactions in solid phase synthesis. It is introduced as a protective group on the side chain of the amino acid to control the synthesis process and the selectivity of the product.
the method for preparing Fmoc-(R)-3-Amino-4-(3-bromo-phenyl)-butyric acid generally adopts a chemical synthesis method, which can be obtained by reacting (R)-3-amino -4-(3-bromophenyl) butyric acid with Fmoc-Cl. Specific operating conditions need to refer to the relevant literature or experimental methods.
Regarding safety information, avoid direct contact with skin, eyes or inhalation of dust during operation. Operate in a well-ventilated laboratory environment and take appropriate personal protective measures, such as wearing protective gloves and goggles. During use or storage, keep the container sealed and avoid high temperature and fire sources. For more detailed recommendations on safe handling and handling, refer to the relevant dangerous goods instructions or contact a professional.
Last Update：2024-04-10 22:29:15
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