(2R,4S)-N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID
Fmoc-trans-4-Hydroxy-D-proline
CAS: 139262-20-7
Molecular Formula: C20H19NO5
(2R,4S)-N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID - Names and Identifiers
(2R,4S)-N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID - Physico-chemical Properties
| Molecular Formula | C20H19NO5 |
| Molar Mass | 353.37 |
| Storage Condition | 2-8℃ |
| Sensitive | Irritant |
| MDL | MFCD01862677 |
(2R,4S)-N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID - Risk and Safety
| Hazard Class | IRRITANT |
(2R,4S)-N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-4-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID - Introduction
(Fmoc-trans-4-hydroxy-D-proline) is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
(Fmoc-trans-4-hydroxy-D-proline) has a chemical formula of C22H19NO5 and a relative molecular mass of 377.39g/mol. It is a white solid, soluble in organic solvents such as dimethyl sulfoxide (DMSO) and methylene chloride. It has a strong formyl protecting group (Fmoc) and a 4-hydroxy group fixed in the molecular structure of D-proline.
Use:
(Fmoc-trans-4-hydroxy-D-proline) is widely used in the synthesis of peptides and proteins in organic synthesis. It can be used as an initial part of the extension of the peptide chain, helping to fix the conformation of the entire peptide chain. In addition, it can also be used in the field of functional peptide design and drug development.
Preparation Method:
(Fmoc-trans-4-hydroxy-D-proline) can be prepared by chemical synthesis. Generally, starting from the synthesis of the amino acid D-proline, and under specific reaction conditions, the Fmoc protecting group is attached to the amino group, followed by the addition of the 4-hydroxy group.
Safety Information:
(Fmoc-trans-4-hydroxy-D-proline) has not been reported to be toxic or dangerous. However, when handling chemical reagents, users should follow laboratory safety procedures, avoid direct contact with skin and eyes, and ensure that they operate in a well-ventilated laboratory environment. In the event of an accident, appropriate first aid measures should be taken immediately and advice from relevant professionals should be consulted.
Nature:
(Fmoc-trans-4-hydroxy-D-proline) has a chemical formula of C22H19NO5 and a relative molecular mass of 377.39g/mol. It is a white solid, soluble in organic solvents such as dimethyl sulfoxide (DMSO) and methylene chloride. It has a strong formyl protecting group (Fmoc) and a 4-hydroxy group fixed in the molecular structure of D-proline.
Use:
(Fmoc-trans-4-hydroxy-D-proline) is widely used in the synthesis of peptides and proteins in organic synthesis. It can be used as an initial part of the extension of the peptide chain, helping to fix the conformation of the entire peptide chain. In addition, it can also be used in the field of functional peptide design and drug development.
Preparation Method:
(Fmoc-trans-4-hydroxy-D-proline) can be prepared by chemical synthesis. Generally, starting from the synthesis of the amino acid D-proline, and under specific reaction conditions, the Fmoc protecting group is attached to the amino group, followed by the addition of the 4-hydroxy group.
Safety Information:
(Fmoc-trans-4-hydroxy-D-proline) has not been reported to be toxic or dangerous. However, when handling chemical reagents, users should follow laboratory safety procedures, avoid direct contact with skin and eyes, and ensure that they operate in a well-ventilated laboratory environment. In the event of an accident, appropriate first aid measures should be taken immediately and advice from relevant professionals should be consulted.
Last Update：2024-04-09 20:45:29
