Boc-D-b-Phe(4-NO2)-OH
Boc-R-3-Amino-3-(4-nitro-phenyl)-propionic acid
CAS:
Molecular Formula: C14H18N2O6
Boc-D-b-Phe(4-NO2)-OH - Names and Identifiers
Boc-D-b-Phe(4-NO2)-OH - Physico-chemical Properties
| Molecular Formula | C14H18N2O6 |
| Molar Mass | 310.3 |
| Density | 1.288±0.06 g/cm3(Predicted) |
| Boling Point | 503.0±50.0 °C(Predicted) |
| pKa | 4.14±0.10(Predicted) |
| Storage Condition | 2-8°C |
Boc-D-b-Phe(4-NO2)-OH - Introduction
Boc-R-3-Amino-3-(4-nitro-phenyl)-propionic acid(Boc-R-3-Amino-3-(4-nitro-phenyl)-propionic acid) is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance: White crystalline solid.
-Molecular formula: C16H20N2O6.
-Molecular weight: 332.34g/mol.
-Melting point: about 135-137°C.
-Solubility: Soluble in some organic solvents, such as ethanol and dichloromethane.
Use:
- Boc-R-3-Amino-3-(4-nitro-phenyl)-propionic acid is a commonly used reagent in organic synthesis, which is widely used in the field of medicinal chemistry research and synthetic chemistry.
-It can be used as an important intermediate in the construction and modification of drug molecules, synthetic peptides and protein chemical modification.
Preparation Method:
- Boc-R-3-Amino-3-(4-nitro-phenyl)-propionic acid is generally prepared by chemical synthesis. Specific methods are optimized according to laboratory conditions and needs, but common synthetic routes include the following steps:
1. first synthesis of intermediates of target compounds, such as nitrobenzaldehyde.
2. The intermediate is reacted with an appropriate linking reagent to form Boc-R-3-amino -3-(4-nitrophenyl) propionic acid.
3. Finally, the Boc protecting group can be removed to obtain the final Boc-R-3-amino -3-(4-nitrophenyl) propionic acid.
Safety Information:
- Boc-R-3-Amino-3-(4-nitro-phenyl)-The safety and risk of propionic acid should be assessed on a case-by-case basis.
-When working in a laboratory, take appropriate safety measures, such as wearing personal protective equipment (e. g., lab suits and gloves), operating in well-ventilated conditions, and following safe chemical practices.
-If you need to use or handle Boc-R-3-amino -3-(4-nitrophenyl) propionic acid, it is recommended to refer to the relevant safety data sheet and follow the safety operation recommendations provided by the supplier.
Nature:
-Appearance: White crystalline solid.
-Molecular formula: C16H20N2O6.
-Molecular weight: 332.34g/mol.
-Melting point: about 135-137°C.
-Solubility: Soluble in some organic solvents, such as ethanol and dichloromethane.
Use:
- Boc-R-3-Amino-3-(4-nitro-phenyl)-propionic acid is a commonly used reagent in organic synthesis, which is widely used in the field of medicinal chemistry research and synthetic chemistry.
-It can be used as an important intermediate in the construction and modification of drug molecules, synthetic peptides and protein chemical modification.
Preparation Method:
- Boc-R-3-Amino-3-(4-nitro-phenyl)-propionic acid is generally prepared by chemical synthesis. Specific methods are optimized according to laboratory conditions and needs, but common synthetic routes include the following steps:
1. first synthesis of intermediates of target compounds, such as nitrobenzaldehyde.
2. The intermediate is reacted with an appropriate linking reagent to form Boc-R-3-amino -3-(4-nitrophenyl) propionic acid.
3. Finally, the Boc protecting group can be removed to obtain the final Boc-R-3-amino -3-(4-nitrophenyl) propionic acid.
Safety Information:
- Boc-R-3-Amino-3-(4-nitro-phenyl)-The safety and risk of propionic acid should be assessed on a case-by-case basis.
-When working in a laboratory, take appropriate safety measures, such as wearing personal protective equipment (e. g., lab suits and gloves), operating in well-ventilated conditions, and following safe chemical practices.
-If you need to use or handle Boc-R-3-amino -3-(4-nitrophenyl) propionic acid, it is recommended to refer to the relevant safety data sheet and follow the safety operation recommendations provided by the supplier.
Last Update：2024-04-09 21:00:56
