Fmoc-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoicacid
Fmoc-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoicacid
CAS: 1217833-77-6
Molecular Formula: C21H23NO5
Fmoc-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoicacid - Names and Identifiers
Fmoc-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoicacid - Physico-chemical Properties
| Molecular Formula | C21H23NO5 |
| Molar Mass | 369.41 |
| Density | 1.271±0.06 g/cm3(Predicted) |
| Boling Point | 601.8±55.0 °C(Predicted) |
| pKa | 3.51±0.23(Predicted) |
| Storage Condition | 2-8℃ |
| Sensitive | Irritant |
| MDL | MFCD02682583 |
Fmoc-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoicacid - Risk and Safety
| Hazard Class | IRRITANT |
Fmoc-(2R,3S)-2-amino-3-hydroxy-4-methylpentanoicacid - Introduction
Fmoc-(2R,3S)-is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
Fmoc-(2R,3S)-is a white or off-white solid. It is soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and dichloromethane. Its molecular formula is C17H19NO4 and its relative molecular mass is 309.34. It is a chiral compound with a 2R,3S stereo configuration.
Use:
Fmoc-(2R,3S)-is a commonly used amino acid protecting group used in solid phase synthesis. It can be combined with other amino acid residues for solid phase synthesis by photochemical or chemical methods. In polypeptide synthesis, the Fmoc group is typically used to protect the amine group of an amino acid.
Preparation Method:
Fmoc-(2R,3S)-The synthesis of fmoc-(2R,3S)-can be carried out through a multi-step reaction. A common preparation method is to start from alanine, through a series of reactions, including substitution reaction and protective group conversion reaction, to obtain the target product.
Safety Information:
Fmoc-(2R,3S)-is relatively safe in most cases, but should be used with caution. It can be harmful to health, especially to the skin, eyes and respiratory tract. Wear appropriate protective equipment, such as gloves, safety glasses and protective masks. Avoid inhaling its dust or contact with skin and eyes during operation. If you come into contact with this compound, rinse immediately with plenty of water and seek medical help.
Nature:
Fmoc-(2R,3S)-is a white or off-white solid. It is soluble in some organic solvents, such as dimethyl sulfoxide (DMSO) and dichloromethane. Its molecular formula is C17H19NO4 and its relative molecular mass is 309.34. It is a chiral compound with a 2R,3S stereo configuration.
Use:
Fmoc-(2R,3S)-is a commonly used amino acid protecting group used in solid phase synthesis. It can be combined with other amino acid residues for solid phase synthesis by photochemical or chemical methods. In polypeptide synthesis, the Fmoc group is typically used to protect the amine group of an amino acid.
Preparation Method:
Fmoc-(2R,3S)-The synthesis of fmoc-(2R,3S)-can be carried out through a multi-step reaction. A common preparation method is to start from alanine, through a series of reactions, including substitution reaction and protective group conversion reaction, to obtain the target product.
Safety Information:
Fmoc-(2R,3S)-is relatively safe in most cases, but should be used with caution. It can be harmful to health, especially to the skin, eyes and respiratory tract. Wear appropriate protective equipment, such as gloves, safety glasses and protective masks. Avoid inhaling its dust or contact with skin and eyes during operation. If you come into contact with this compound, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-10 22:29:15
