161220-53-7
Fmoc-Ala-Ala-Pro-OH
CAS: 161220-53-7
Molecular Formula: C26H29N3O6
161220-53-7 - Names and Identifiers
161220-53-7 - Physico-chemical Properties
| Molecular Formula | C26H29N3O6 |
| Molar Mass | 479.52 |
| Density | 1.311 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD01862421 |
161220-53-7 - Introduction
Fmoc-Ala-Ala-Pro-OH, full name is a peptide compound. The following is a description of the nature, use, preparation and safety information of the Fmoc-Ala-Ala-Pro-OH:
Nature:
Fmoc-Ala-Ala-Pro-OH is a white crystalline solid with good solubility. It has high solubility in organic solvents (such as dimethylformamide and dichloromethane) and low solubility in water.
Use:
Fmoc-Ala-Ala-Pro-OH is a commonly used peptide synthesis intermediate. It can be used in the synthesis of peptide chains with Fmoc-Ala-Ala-Pro structure as a protecting group to protect the amino acid functional groups in the peptide chain from the reaction. In addition, Fmoc-Ala-Ala-Pro-OH can also be used in biochemical research, for the synthesis and study of peptide compounds with Ala-Ala-Pro sequence, to explore its biological activity and physiological function.
Preparation Method:
The preparation method of Fmoc-Ala-Ala-Pro-OH usually adopts solid phase synthesis technology. First, the Fmoc protecting group was coupled with amino acid residues such as Alanine(Ala) and Proline(Pro) by successive reactions on a solid-phase synthetic resin to obtain a complete peptide chain. Finally, the protecting group is removed by an appropriate reaction to give the target compound Fmoc-Ala-Ala-Pro-OH.
Safety Information:
Fmoc-Ala-Ala-Pro-OH are chemicals and need to pay attention to safe operation. Wear protective glasses and gloves when using, and ensure that the operation is carried out in a well-ventilated place. Avoid inhaling dust or contact with skin. If contact or aspiration occurs, rinse immediately with plenty of water and seek medical attention.
Nature:
Fmoc-Ala-Ala-Pro-OH is a white crystalline solid with good solubility. It has high solubility in organic solvents (such as dimethylformamide and dichloromethane) and low solubility in water.
Use:
Fmoc-Ala-Ala-Pro-OH is a commonly used peptide synthesis intermediate. It can be used in the synthesis of peptide chains with Fmoc-Ala-Ala-Pro structure as a protecting group to protect the amino acid functional groups in the peptide chain from the reaction. In addition, Fmoc-Ala-Ala-Pro-OH can also be used in biochemical research, for the synthesis and study of peptide compounds with Ala-Ala-Pro sequence, to explore its biological activity and physiological function.
Preparation Method:
The preparation method of Fmoc-Ala-Ala-Pro-OH usually adopts solid phase synthesis technology. First, the Fmoc protecting group was coupled with amino acid residues such as Alanine(Ala) and Proline(Pro) by successive reactions on a solid-phase synthetic resin to obtain a complete peptide chain. Finally, the protecting group is removed by an appropriate reaction to give the target compound Fmoc-Ala-Ala-Pro-OH.
Safety Information:
Fmoc-Ala-Ala-Pro-OH are chemicals and need to pay attention to safe operation. Wear protective glasses and gloves when using, and ensure that the operation is carried out in a well-ventilated place. Avoid inhaling dust or contact with skin. If contact or aspiration occurs, rinse immediately with plenty of water and seek medical attention.
Last Update：2024-04-09 21:01:54
