FMOC-(R)-3-AMINO-4-(2-FURYL)BUTANOIC ACID
Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid
CAS: 270596-34-4
Molecular Formula: C23H21NO5
FMOC-(R)-3-AMINO-4-(2-FURYL)BUTANOIC ACID - Names and Identifiers
FMOC-(R)-3-AMINO-4-(2-FURYL)BUTANOIC ACID - Physico-chemical Properties
| Molecular Formula | C23H21NO5 |
| Molar Mass | 391.42 |
| Density | 1.292±0.06 g/cm3(Predicted) |
| Boling Point | 616.4±55.0 °C(Predicted) |
| pKa | 4.34±0.10(Predicted) |
FMOC-(R)-3-AMINO-4-(2-FURYL)BUTANOIC ACID - Risk and Safety
| Hazard Class | IRRITANT |
FMOC-(R)-3-AMINO-4-(2-FURYL)BUTANOIC ACID - Introduction
Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid is an organic compound commonly used in the synthesis of peptides and proteins. It has the following properties:
1. Appearance: white solid
2. molecular formula: C21H19NO4
3. Molecular weight: 353.38g/mol
4. solubility: soluble in some organic solvents such as dichloromethane, dimethyl sulfoxide and chloroform, slightly insoluble in water.
The main use of Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid is as a protecting group in solid phase synthesis, which can be used in the synthesis of peptides and proteins. It can be coupled with other amino acids or peptide chains through chemical reactions to construct complex peptide sequences.
The method for preparing Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid is generally an organic synthesis method. The specific preparation steps may be slightly complicated, requiring the use of multiple chemical reagents and conditions, and are generally synthesized in conjunction with existing synthesis schemes.
For safety information, Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid is not currently classified as a hazardous substance, but it is important to follow laboratory safety practices, wear appropriate protective equipment, avoid contact with skin and eyes, and avoid inhalation or ingestion. In case of contact, flush with water and seek medical assistance.
1. Appearance: white solid
2. molecular formula: C21H19NO4
3. Molecular weight: 353.38g/mol
4. solubility: soluble in some organic solvents such as dichloromethane, dimethyl sulfoxide and chloroform, slightly insoluble in water.
The main use of Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid is as a protecting group in solid phase synthesis, which can be used in the synthesis of peptides and proteins. It can be coupled with other amino acids or peptide chains through chemical reactions to construct complex peptide sequences.
The method for preparing Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid is generally an organic synthesis method. The specific preparation steps may be slightly complicated, requiring the use of multiple chemical reagents and conditions, and are generally synthesized in conjunction with existing synthesis schemes.
For safety information, Fmoc-(R)-3-Amino-4-(2-furyl)-butyric acid is not currently classified as a hazardous substance, but it is important to follow laboratory safety practices, wear appropriate protective equipment, avoid contact with skin and eyes, and avoid inhalation or ingestion. In case of contact, flush with water and seek medical assistance.
Last Update：2024-04-10 22:29:15
