N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE
Boc-pentafluoro-D-Phe-OH
CAS: 136207-26-6
Molecular Formula: C14H14F5NO4
N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE - Names and Identifiers
| Name | Boc-pentafluoro-D-Phe-OH |
| Synonyms | Boc-D-Phe(5F)-OH RARECHEM BK PT 0107 Boc-pentafluoro-D-Phe-OH Boc-D-Pentafluorophenylalanine Boc-pentafluoro-D-phenylalanine Boc-3-(Pentafluorophenyl)-D-alanine (Tert-Butoxy)Carbonyl D-Pentafluorophe N-ALPHA-T-BUTOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE (R)-Boc-2-amino-3-(pentafluorophenyl)propionic acid N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE (R)-2-TERT-BUTOXYCARBONYLAMINO-3-PENTAFLUOROPHENYL-PROPIONIC ACID |
| CAS | 136207-26-6 |
| InChI | InChI=1/C14H14F5NO4/c1-14(2,3)24-13(23)20-6(12(21)22)4-5-7(15)9(17)11(19)10(18)8(5)16/h6H,4H2,1-3H3,(H,20,23)(H,21,22)/t6-/m0/s1 |
N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE - Physico-chemical Properties
| Molecular Formula | C14H14F5NO4 |
| Molar Mass | 355.26 |
| Density | 1.422±0.06 g/cm3(Predicted) |
| Boling Point | 411.1±45.0 °C(Predicted) |
| Flash Point | 202.4°C |
| Vapor Presure | 1.7E-07mmHg at 25°C |
| pKa | 3.70±0.20(Predicted) |
| Storage Condition | Sealed in dry,Store in freezer, under -20°C |
| Refractive Index | 1.476 |
N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| WGK Germany | 3 |
| Hazard Note | Harmful/Irritant/Keep Cold |
N-ALPHA-TERT-BUTYLOXYCARBONYL-D-PENTAFLUOROPHENYLALANINE - Introduction
N-tert-butoxycarbonyl-D-pentafluorophenylalanine is an organic compound with the chemical formula C13H16F5NO4. It is a solid with a white to yellowish crystal form. It is a kind of amino acid derivatives, which plays an important role in biochemical research by changing the structure and function.
N-tert-Butoxycarbonyl-D-pentafluorophenylalanine is widely used in drug synthesis and biochemical research. It can be used as a substrate for the preparation of peptide drugs, protein engineering and enzyme-catalyzed reactions. It can also be used for chemical reactions such as drug crosslinking and modification.
The method for preparing N-tert-butoxycarbonyl-D-pentafluorophenylalanine generally involves the following steps: firstly, pentafluorobenzoyl chloride is selected as a starting material, and the target product is finally obtained by esterification reaction with N-tert-butoxycarbonyl-L-phenylalanine. The specific experimental conditions and procedures can be adjusted according to the reaction requirements.
N-tert-butoxycarbonyl-D-pentafluorophenylalanine should comply with certain safety precautions when used. It is an organic compound that may cause irritation to the eyes, skin and respiratory tract. Therefore, appropriate protective equipment, such as laboratory gloves and protective glasses, should be worn during the operation, and a well-ventilated laboratory environment should be maintained. At the same time, the compound should be stored properly to avoid contact with flammable and oxidizing substances to prevent fire and explosion hazards.
N-tert-Butoxycarbonyl-D-pentafluorophenylalanine is widely used in drug synthesis and biochemical research. It can be used as a substrate for the preparation of peptide drugs, protein engineering and enzyme-catalyzed reactions. It can also be used for chemical reactions such as drug crosslinking and modification.
The method for preparing N-tert-butoxycarbonyl-D-pentafluorophenylalanine generally involves the following steps: firstly, pentafluorobenzoyl chloride is selected as a starting material, and the target product is finally obtained by esterification reaction with N-tert-butoxycarbonyl-L-phenylalanine. The specific experimental conditions and procedures can be adjusted according to the reaction requirements.
N-tert-butoxycarbonyl-D-pentafluorophenylalanine should comply with certain safety precautions when used. It is an organic compound that may cause irritation to the eyes, skin and respiratory tract. Therefore, appropriate protective equipment, such as laboratory gloves and protective glasses, should be worn during the operation, and a well-ventilated laboratory environment should be maintained. At the same time, the compound should be stored properly to avoid contact with flammable and oxidizing substances to prevent fire and explosion hazards.
Last Update：2024-04-09 21:11:58
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