[2-(2,4-Difluorophenyl)-2-Hydroxyethyl]-Carbamic Acid 1,1-Dimethylethyl Ester - Names and Identifiers
Name | N-Boc-2-(2,4-difluorophenyl)-2-hydroxyethanamine
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Synonyms | N-Boc-2-(2,4-difluorophenyl)-2-hydroxyethanaMine N-Boc-2-(2,4-difluorophenyl)-2-hydroxyethanamine [2-(2,4-Difluoro-Phenyl)-2-Hydroxy-Ethyl]-Carbamic Acid Tert-Butyl Ester [2-(2,4-DIFLUORO-PHENYL)-2-HYDROXY-ETHYL]-CARBAMIC ACID TERT-BUTYL ESTER [2-(2,4-DIFLUOROPHENYL)-2-HYDROXYETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER [2-(2,4-Difluorophenyl)-2-Hydroxyethyl]-Carbamic Acid 1,1-Dimethylethyl Ester Carbamic acid, N-[2-(2,4-difluorophenyl)-2-hydroxyethyl]-, 1,1-dimethylethyl ester
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CAS | 939757-31-0
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[2-(2,4-Difluorophenyl)-2-Hydroxyethyl]-Carbamic Acid 1,1-Dimethylethyl Ester - Physico-chemical Properties
[2-(2,4-Difluorophenyl)-2-Hydroxyethyl]-Carbamic Acid 1,1-Dimethylethyl Ester - Introduction
N-Boc-2-(2,4-difluorophenyl)-2-hydroxyethanamine(N-Boc-2-(2,4-difluorophenyl)-2-hydroxyethanamine) is an organic compound that has the following properties:
1. appearance: white or white solid.
2. Structure: This is a secondary amine containing a protecting group (Boc group), which has a hydroxyl group and a 2,4-difluorophenyl group attached to the amino group in the molecule.
3. melting point: about 70-80 ℃.
4. Solubility: It can be dissolved in some organic solvents, such as dimethylformamide (DMF) and dichloromethane (DCM).
N-Boc-2-(2,4-difluorophenyl)-2-hydroxyethanamine has the following main applications:
1. Organic synthesis: As an intermediate, it can be used to prepare other organic compounds. For example, useful compounds can be further synthesized by deprotecting the Boc group and performing a chemical reaction.
2. Drug research: The compound may be used in drug research and development, and used to synthesize new drug molecules.
The synthesis of N-Boc-2-(2,4-difluorophenyl)-2-hydroxyethanamine can usually be carried out as follows:
1. First, a hydroxyl group and a difluorophenyl group are introduced by an appropriate reaction.
2. Next, a protecting group (Boc group) is introduced to the hydroxyl group.
3. Finally, the pure product is obtained by appropriate purification and crystallization steps.
Regarding the safety information of this compound, it is necessary to follow the routine organic chemistry laboratory safety operations when using and handling. Pay attention to prevent inhalation, ingestion or skin contact, avoid inhaling dust, and maintain good ventilation conditions. Wear appropriate personal protective equipment, such as gloves, safety glasses and lab clothes. If necessary, the operation should be carried out in the safety cabinet. In addition, specific assessments of the safety and toxicity of the compound should be made based on its specific use and relevant data for the chemical in question.
Last Update:2024-04-09 21:54:55