FMOC-L-PENTAFLUOROPHE
Fmoc-L-Pentafluorophe
CAS: 205526-32-5
Molecular Formula: C24H16F5NO4
FMOC-L-PENTAFLUOROPHE - Names and Identifiers
FMOC-L-PENTAFLUOROPHE - Physico-chemical Properties
| Molecular Formula | C24H16F5NO4 |
| Molar Mass | 477.38 |
| Density | 1.471±0.06 g/cm3(Predicted) |
| Boling Point | 602.9±55.0 °C(Predicted) |
| pKa | 3.59±0.20(Predicted) |
| Storage Condition | 2-8°C |
FMOC-L-PENTAFLUOROPHE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| WGK Germany | 3 |
| Hazard Note | Harmful/Irritant/Keep Cold |
FMOC-L-PENTAFLUOROPHE - Introduction
Fmoc-L-Pentafluorophe is an organic compound that has the following properties, uses, methods of manufacture and safety information:
Nature:
Fmoc-L-Pentafluorophe is a white crystalline powder with high stability. It is an amino acid derivative and is widely used in biochemistry and medicinal chemistry.
Use:
Fmoc-L-Pentafluorophe are commonly used in the synthesis of peptides, proteins and drug molecules. It is a protecting group in peptide synthesis, and the sequence of peptide chains can be established by peptide synthesis with Fmoc-protecting groups. The introduction of the amino acid can also change the chemical properties, stability and solubility of the peptide, which is of great significance to drug research.
Method:
The preparation of Fmoc-L-Pentafluorophe is generally carried out by an organic synthesis method. The method mainly includes the steps of chemical reaction, separation and purification and crystallization. Detailed descriptions of specific synthetic methods can be found in handbooks of organic chemistry and in the scientific literature.
Safety Information:
Fmoc-L-Pentafluorophe as laboratory reagents should be operated in appropriate facilities and in strict compliance with relevant safety procedures. It may be irritating and toxic, and care should be taken to avoid inhalation, ingestion, or skin contact. Appropriate personal protective equipment, such as lab gloves, safety glasses and lab coats, should be worn during use. After use, it should be properly stored to avoid mixing with other chemicals. Detailed safety information can be found in the relevant safety data sheet (SDS).
Nature:
Fmoc-L-Pentafluorophe is a white crystalline powder with high stability. It is an amino acid derivative and is widely used in biochemistry and medicinal chemistry.
Use:
Fmoc-L-Pentafluorophe are commonly used in the synthesis of peptides, proteins and drug molecules. It is a protecting group in peptide synthesis, and the sequence of peptide chains can be established by peptide synthesis with Fmoc-protecting groups. The introduction of the amino acid can also change the chemical properties, stability and solubility of the peptide, which is of great significance to drug research.
Method:
The preparation of Fmoc-L-Pentafluorophe is generally carried out by an organic synthesis method. The method mainly includes the steps of chemical reaction, separation and purification and crystallization. Detailed descriptions of specific synthetic methods can be found in handbooks of organic chemistry and in the scientific literature.
Safety Information:
Fmoc-L-Pentafluorophe as laboratory reagents should be operated in appropriate facilities and in strict compliance with relevant safety procedures. It may be irritating and toxic, and care should be taken to avoid inhalation, ingestion, or skin contact. Appropriate personal protective equipment, such as lab gloves, safety glasses and lab coats, should be worn during use. After use, it should be properly stored to avoid mixing with other chemicals. Detailed safety information can be found in the relevant safety data sheet (SDS).
Last Update：2024-04-09 19:05:47
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