210282-31-8
fmoc-l-3-iodophenylalanine
CAS: 210282-31-8
Molecular Formula: C24H20INO4
210282-31-8 - Names and Identifiers
210282-31-8 - Physico-chemical Properties
| Molecular Formula | C24H20INO4 |
| Molar Mass | 513.32 |
| Density | 1.577±0.06 g/cm3(Predicted) |
| Boling Point | 674.1±55.0 °C(Predicted) |
| pKa | 3.71±0.10(Predicted) |
| Storage Condition | Keep in dark place,Sealed in dry,2-8°C |
| Sensitive | Irritant |
| MDL | MFCD01632252 |
210282-31-8 - Risk and Safety
| Hazard Class | IRRITANT |
210282-31-8 - Introduction
fmoc-l-3-iodophenylalanine is an amino acid derivative with the following properties:
1. Appearance: White crystalline solid.
2. Molecular formula: C24H18INO4.
3. Molecular weight: 484.31g/mol.
4. Melting Point: 172-174 ° C.
5. Solubility: Soluble in organic solvents such as dimethyl sulfoxide and dichloromethane.
fmoc-l-3-iodophenylalanine are commonly used in biochemistry and medicinal chemistry. It is mainly used for protecting group strategy in peptide synthesis, and can be used as protecting amino acid in peptide synthesis, so as to control the chemical reaction of specific site. In addition, it can also be used for synthesis and structural modification in drug development.
The fmoc-l-3-iodophenylalanine can be produced by chemical synthesis. A common method is by first synthesizing L-3-iodophenylalanine and then adding a Fmoc protecting group to its carboxyl group.
Regarding safety information, fmoc-l-3-iodophenylalanine should be used in accordance with relevant laboratory safety procedures. It may be irritating and corrosive to the skin, eyes and mucous membranes. Therefore, appropriate personal protective equipment such as gloves, goggles and laboratory coats should be worn during operation. When storing and handling, it should be placed in a sealed container and away from fire and oxidizing agents.
1. Appearance: White crystalline solid.
2. Molecular formula: C24H18INO4.
3. Molecular weight: 484.31g/mol.
4. Melting Point: 172-174 ° C.
5. Solubility: Soluble in organic solvents such as dimethyl sulfoxide and dichloromethane.
fmoc-l-3-iodophenylalanine are commonly used in biochemistry and medicinal chemistry. It is mainly used for protecting group strategy in peptide synthesis, and can be used as protecting amino acid in peptide synthesis, so as to control the chemical reaction of specific site. In addition, it can also be used for synthesis and structural modification in drug development.
The fmoc-l-3-iodophenylalanine can be produced by chemical synthesis. A common method is by first synthesizing L-3-iodophenylalanine and then adding a Fmoc protecting group to its carboxyl group.
Regarding safety information, fmoc-l-3-iodophenylalanine should be used in accordance with relevant laboratory safety procedures. It may be irritating and corrosive to the skin, eyes and mucous membranes. Therefore, appropriate personal protective equipment such as gloves, goggles and laboratory coats should be worn during operation. When storing and handling, it should be placed in a sealed container and away from fire and oxidizing agents.
Last Update：2024-04-09 20:48:19
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