BOC-D-3,5-DIFLUOROPHE
N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine
CAS: 205445-53-0
Molecular Formula: C14H17F2NO4
BOC-D-3,5-DIFLUOROPHE - Names and Identifiers
| Name | N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine |
| Synonyms | BOC-D-PHE(3,5-DIF)-OH BOC-D-3,5-DIFLUOROPHE Boc-D-3,5-Difluorophe N-Boc-D-Phe(3,5-F2)-OH Boc-D-3,5-Difluoro-phe-OH Boc-D-3,5-Difluorophenylalanine Boc-3,5-Difluoro-D-phenylalanine BOC-3,5-DIFLUORO-D-PHENYLALANINE N-BOC-3,5-DIFLUORO-D-PHENYLALANINE ￡¨R￡-N-Boc-3,5-Difluorophenylalanine N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine Boc-D-Phe(3,5-F2)-OH Boc-3,5-Difluoro-D-Phenylalanine |
| CAS | 205445-53-0 |
| InChI | InChI=1/C14H17F2NO4/c1-14(2,3)21-13(20)17-11(12(18)19)6-8-4-9(15)7-10(16)5-8/h4-5,7,11H,6H2,1-3H3,(H,17,20)(H,18,19)/t11-/m1/s1 |
BOC-D-3,5-DIFLUOROPHE - Physico-chemical Properties
| Molecular Formula | C14H17F2NO4 |
| Molar Mass | 301.29 |
| Density | 1.27g/cm3 |
| Boling Point | 417.6°C at 760 mmHg |
| Flash Point | 206.4°C |
| Vapor Presure | 1.01E-07mmHg at 25°C |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.506 |
BOC-D-3,5-DIFLUOROPHE - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Note | Irritant |
BOC-D-3,5-DIFLUOROPHE - Introduction
N-(tert-butoxycarbonyl)-3,5-difluoro-d-phenylalanine is an organic compound with the chemical formula C14H16F2NO4. It is an organic acid with two fluorine atoms and a protecting group (Boc Group) attached to phenylalanine.
N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine is mainly used in the field of organic synthesis and pharmaceutical research. It can be used as an intermediate in the synthesis of drugs, anti-inflammatory drugs, antiviral drugs and so on. It can also be used to synthesize polypeptides and proteins of specific sequences for biomedical research and drug development.
The preparation method of N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine is usually obtained by chemical synthesis. A common method is to condense a protecting group (Boc group) with 3,5-difluorophenylpropylamine and then react with benzoic anhydride to give the desired product. The preparation process requires certain chemical laboratory techniques and equipment.
When using N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine, attention should be paid to its safety. It is a chemical that has certain toxicity and irritation. Avoid inhalation, ingestion or skin contact. Chemical protective gloves, goggles and protective clothing should be worn during operation. At the same time, it should be operated in a well-ventilated place to avoid dust and gas. Waste should be disposed of in accordance with local regulations to avoid pollution to the environment.
N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine is mainly used in the field of organic synthesis and pharmaceutical research. It can be used as an intermediate in the synthesis of drugs, anti-inflammatory drugs, antiviral drugs and so on. It can also be used to synthesize polypeptides and proteins of specific sequences for biomedical research and drug development.
The preparation method of N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine is usually obtained by chemical synthesis. A common method is to condense a protecting group (Boc group) with 3,5-difluorophenylpropylamine and then react with benzoic anhydride to give the desired product. The preparation process requires certain chemical laboratory techniques and equipment.
When using N-(tert-butoxycarbonyl)-3,5-difluoro-D-phenylalanine, attention should be paid to its safety. It is a chemical that has certain toxicity and irritation. Avoid inhalation, ingestion or skin contact. Chemical protective gloves, goggles and protective clothing should be worn during operation. At the same time, it should be operated in a well-ventilated place to avoid dust and gas. Waste should be disposed of in accordance with local regulations to avoid pollution to the environment.
Last Update：2024-04-09 21:11:58
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Product Name: Boc-D-3,5-Difluorophenylalanine Request for quotation
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CAS: 205445-53-0
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