167993-21-7
Boc-L-2-Trifluoromethylphe
CAS: 167993-21-7
Molecular Formula: C15H18F3NO4
167993-21-7 - Names and Identifiers
| Name | Boc-L-2-Trifluoromethylphe |
| Synonyms | BOC-PHE(2-CF 3)-OH BOC-L-PHE(2-CF3)-OH Boc-L-2-Trifluoromethylphe BOC-L-2-TRIFLUOROMETHYLPHE BOC-L-2-Trifluoromethylphe BOC-L-PHE(2-TRIFLUOROMETHYL)-OH BOC-L-2-TRIFLUOROMETHYLPHENYLALANINE boc-l-2-trifluoromethylphenylalanine Boc-2-Trifluoromethyl-L-phenylalanine N-BOC-L-2-(trifluoromethyl)phenylalanine N-(tert-butoxycarbonyl)-2-(trifluoromethyl)-D-phenylalanine N-(tert-butoxycarbonyl)-2-(trifluoromethyl)-L-phenylalanine 2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-[2-(trifluoromethyl)phenyl]propanoic acid |
| CAS | 167993-21-7 |
| InChI | InChI=1/C15H18F3NO4/c1-14(2,3)23-13(22)19-11(12(20)21)8-9-6-4-5-7-10(9)15(16,17)18/h4-7,11H,8H2,1-3H3,(H,19,22)(H,20,21)/t11-/m1/s1 |
167993-21-7 - Physico-chemical Properties
| Molecular Formula | C15H18F3NO4 |
| Molar Mass | 333.3 |
| Density | 1.271±0.06 g/cm3(Predicted) |
| Boling Point | 421.8±45.0 °C(Predicted) |
| Flash Point | 208.9°C |
| Vapor Presure | 7.2E-08mmHg at 25°C |
| pKa | 3.76±0.11(Predicted) |
| Storage Condition | Sealed in dry,Store in freezer, under -20°C |
| Refractive Index | 1.487 |
167993-21-7 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| WGK Germany | 3 |
| Hazard Class | IRRITANT |
167993-21-7 - Introduction
Boc-L-2-Trifluoromethylphe is an organic compound also known as N-tert-butoxycarbonyl-L-2-trifluoromethylphenylalanine. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: White crystalline powder
-molecular formula: C14H14F3NO4
-Molecular weight: 321.26g/mol
-Melting Point: about 110-114 ° C
-Solubility: Soluble in organic solvents such as dichloromethane, ethanol and acetone, insoluble in water
Use:
- Boc-L-2-Trifluoromethylphe is commonly used as an amino acid protecting group in organic synthesis for the synthesis of peptide compounds.
-It can be used as an important raw material for synthetic drugs, pharmaceutical intermediates and biochemical research.
Method:
The synthesis of Boc-L-2-Trifluoromethylphe usually goes through the following steps:
1. The Boc-L-2-Trifluoromethylphe was obtained by reacting L-2-trifluoromethylphenylalanine with tert-butyl to obtain urea (BOC-OSU) and forming a temporary protecting group under basic conditions.
Safety Information:
- Boc-L-2-Trifluoromethylphe there is no obvious toxicity to human body under general operating conditions, but it is still necessary to pay attention to safe operation.
-Avoid inhaling dust or skin contact and wear appropriate protective equipment.
-When using or handling this compound, ensure that the operating environment is well ventilated.
-storage should be sealed in a dry, cool place, away from the fire and oxidant.
Nature:
-Appearance: White crystalline powder
-molecular formula: C14H14F3NO4
-Molecular weight: 321.26g/mol
-Melting Point: about 110-114 ° C
-Solubility: Soluble in organic solvents such as dichloromethane, ethanol and acetone, insoluble in water
Use:
- Boc-L-2-Trifluoromethylphe is commonly used as an amino acid protecting group in organic synthesis for the synthesis of peptide compounds.
-It can be used as an important raw material for synthetic drugs, pharmaceutical intermediates and biochemical research.
Method:
The synthesis of Boc-L-2-Trifluoromethylphe usually goes through the following steps:
1. The Boc-L-2-Trifluoromethylphe was obtained by reacting L-2-trifluoromethylphenylalanine with tert-butyl to obtain urea (BOC-OSU) and forming a temporary protecting group under basic conditions.
Safety Information:
- Boc-L-2-Trifluoromethylphe there is no obvious toxicity to human body under general operating conditions, but it is still necessary to pay attention to safe operation.
-Avoid inhaling dust or skin contact and wear appropriate protective equipment.
-When using or handling this compound, ensure that the operating environment is well ventilated.
-storage should be sealed in a dry, cool place, away from the fire and oxidant.
Last Update：2024-04-09 02:00:42
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View History
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