BOC-L-2-fluorophenylalanine
BOC-L-2-fluorophenylalanine
CAS: 114873-00-6
Molecular Formula: C14H18FNO4
BOC-L-2-fluorophenylalanine - Names and Identifiers
| Name | BOC-L-2-fluorophenylalanine |
| Synonyms | BOC-PHE(O-F)-OH BOC-Phe(2-F)-OH BOC-PHE(2-F)-OH BOC-L-2-FLUOROPHE BOC-L-PHE(2-F)-OH Boc-L-2-Fluorophe BOC-O-FLUORO-PHE-OH BOC-L-2-fluorophenylalanine BOC-L-2-FLUOROPHENYLALANINE BOC-2-fluoro-L-phenylalanine tert-Butoxycarbonyl-L-2-fluorophenylalanine N-TERT-BUTOXYCARBONYL-2-FLUOROPHENYL-L-ALANINE N-(tert-butoxycarbonyl)-2-fluoro-L-phenylalanine N-(tert-butoxycarbonyl)-2-fluoro-D-phenylalanine BOC-(S)-2-AMINO-3-(2'-FLUOROPHENYL)PROPANOIC ACID (2S)-2-[(tert-butoxycarbonyl)amino]-3-(2-fluorophenyl)propanoate |
| CAS | 114873-00-6 |
| EINECS | 220-105-7 |
| InChI | InChI=1/C14H18FNO4/c1-14(2,3)20-13(19)16-11(12(17)18)8-9-6-4-5-7-10(9)15/h4-7,11H,8H2,1-3H3,(H,16,19)(H,17,18)/t11-/m1/s1 |
BOC-L-2-fluorophenylalanine - Physico-chemical Properties
| Molecular Formula | C14H18FNO4 |
| Molar Mass | 283.3 |
| Density | 1.1918 (estimate) |
| Melting Point | 92-96°C |
| Boling Point | 427.3±40.0 °C(Predicted) |
| Specific Rotation(α) | 10 º (c=1,EtOAc) |
| Flash Point | 212.2°C |
| Vapor Presure | 4.61E-08mmHg at 25°C |
| Appearance | Solid |
| BRN | 5347990 |
| pKa | 3.87±0.11(Predicted) |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.517 |
| MDL | MFCD00672520 |
| Physical and Chemical Properties | Melting point 94°C specific rotation 10 ° (c = 1,EtOAc) |
BOC-L-2-fluorophenylalanine - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| Hazard Note | Irritant/Keep Cold |
BOC-L-2-fluorophenylalanine - Introduction
BOC-L-2-Fluorophenylalanine is a chemical compound, which is called tert-butyloxycarbonyl-L-2-fluorophenylalanine in English. The following is an introduction to its nature, use, preparation and safety information:
Nature:
BOC-L-2-Fluorophenylalanine is a crystalline solid with a fluorine atom in its chemical structure. It is a white to light yellow solid, almost insoluble in water, but in some organic solvents such as alcohol and dimethyl sulfoxide solubility is good. It can be hydrolyzed by an enzyme catalyst to obtain the biologically active L-2-fluorophenylalanine.
Use:
BOC-L-2-Fluorophenylalanine is commonly used as an intermediate in the field of organic synthesis. It can be used as a raw material in the synthesis of drugs, peptides and bioactive molecules. In addition, it can also be used for labels and probes in research and drug development.
Method:
The preparation of BOC-L-2-fluorophenylalanine is usually completed by chemical synthesis methods. Specifically, BOC-L-2-fluorophenylalanine can be synthesized by reacting 2-fluoropropionic acid and tert-butylchloroformate as raw materials under appropriate conditions.
Safety Information:
BOC-L-2-Fluorophenylalanine is generally considered to be relatively safe under conventional use conditions. However, as a chemical, any operation should follow safe practices, such as wearing appropriate protective equipment (such as laboratory gloves and goggles) and avoiding ingestion or contact with skin and eyes. In addition, it should be stored in a dry, ventilated and away from fire sources. In case of any accident, seek medical help immediately.
Nature:
BOC-L-2-Fluorophenylalanine is a crystalline solid with a fluorine atom in its chemical structure. It is a white to light yellow solid, almost insoluble in water, but in some organic solvents such as alcohol and dimethyl sulfoxide solubility is good. It can be hydrolyzed by an enzyme catalyst to obtain the biologically active L-2-fluorophenylalanine.
Use:
BOC-L-2-Fluorophenylalanine is commonly used as an intermediate in the field of organic synthesis. It can be used as a raw material in the synthesis of drugs, peptides and bioactive molecules. In addition, it can also be used for labels and probes in research and drug development.
Method:
The preparation of BOC-L-2-fluorophenylalanine is usually completed by chemical synthesis methods. Specifically, BOC-L-2-fluorophenylalanine can be synthesized by reacting 2-fluoropropionic acid and tert-butylchloroformate as raw materials under appropriate conditions.
Safety Information:
BOC-L-2-Fluorophenylalanine is generally considered to be relatively safe under conventional use conditions. However, as a chemical, any operation should follow safe practices, such as wearing appropriate protective equipment (such as laboratory gloves and goggles) and avoiding ingestion or contact with skin and eyes. In addition, it should be stored in a dry, ventilated and away from fire sources. In case of any accident, seek medical help immediately.
Last Update：2024-04-09 20:52:54
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