Fmoc-D-tert-leucine
Fmoc-tBu-D-Gly-OH
CAS: 198543-64-5
Molecular Formula: C21H23NO4
Fmoc-D-tert-leucine - Names and Identifiers
Fmoc-D-tert-leucine - Physico-chemical Properties
| Molecular Formula | C21H23NO4 |
| Molar Mass | 353.41 |
| Density | 1.209±0.06 g/cm3(Predicted) |
| Melting Point | 126-130°C |
| Boling Point | 554.1±33.0 °C(Predicted) |
| pKa | 3.92±0.10(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
Fmoc-D-tert-leucine - Risk and Safety
| WGK Germany | WGK 2 water endanger |
| HS Code | 2924 29 70 |
| Hazard Class | IRRITANT |
Fmoc-D-tert-leucine - Introduction
Fmoc-tBu-D-Gly-OH is an amino acid derivative with a variety of properties and applications. The following is a description of its nature, use, preparation and safety information:
Nature:
1. Chemical properties: Fmoc-tBu-D-Gly-OH is a compound with potential chiral center.
2. Solubility: soluble in organic solvents such as dimethyl sulfoxide (DMSO), dichloromethane, slightly soluble in ethanol and methanol.
Use:
1. In solid phase synthesis: Fmoc-tBu-D-Gly-OH is commonly used in solid phase synthesis, especially in polypeptide synthesis, as one of the amino acid components. It can be used to construct highly specific and functional polypeptides.
2. Drug development: Due to its chiral structure and special chemical properties, Fmoc-tBu-D-Gly-OH is also widely used in the field of drug development, especially in the synthesis of new drugs and the construction of drug molecules.
3. Biochemical research: Fmoc-tBu-D-Gly-OH can also be used for protein synthesis and modification in biochemical research.
Method:
The production method of Fmoc-tBu-D-Gly-OH is usually obtained by chemical synthesis. Specific preparation steps can be found through literature or patents.
Safety Information:
1. Fmoc-tBu-D-Gly-OH are laboratory reagents, which are irritating and sensitive. Please take necessary protective measures when operating in the laboratory, including wearing protective gloves and glasses.
2. During storage and handling, it is necessary to avoid contact with strong oxidants and strong acids to avoid dangerous chemical reactions.
3. Not recommended for internal human body applications, only for laboratory research purposes.
Please note that when using any chemical and laboratory reagents, always follow laboratory safety guidelines and operate under the guidance of professionals.
Nature:
1. Chemical properties: Fmoc-tBu-D-Gly-OH is a compound with potential chiral center.
2. Solubility: soluble in organic solvents such as dimethyl sulfoxide (DMSO), dichloromethane, slightly soluble in ethanol and methanol.
Use:
1. In solid phase synthesis: Fmoc-tBu-D-Gly-OH is commonly used in solid phase synthesis, especially in polypeptide synthesis, as one of the amino acid components. It can be used to construct highly specific and functional polypeptides.
2. Drug development: Due to its chiral structure and special chemical properties, Fmoc-tBu-D-Gly-OH is also widely used in the field of drug development, especially in the synthesis of new drugs and the construction of drug molecules.
3. Biochemical research: Fmoc-tBu-D-Gly-OH can also be used for protein synthesis and modification in biochemical research.
Method:
The production method of Fmoc-tBu-D-Gly-OH is usually obtained by chemical synthesis. Specific preparation steps can be found through literature or patents.
Safety Information:
1. Fmoc-tBu-D-Gly-OH are laboratory reagents, which are irritating and sensitive. Please take necessary protective measures when operating in the laboratory, including wearing protective gloves and glasses.
2. During storage and handling, it is necessary to avoid contact with strong oxidants and strong acids to avoid dangerous chemical reactions.
3. Not recommended for internal human body applications, only for laboratory research purposes.
Please note that when using any chemical and laboratory reagents, always follow laboratory safety guidelines and operate under the guidance of professionals.
Last Update：2024-04-09 15:17:54
