[2-(2-chlorophenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester - Names and Identifiers
Name | N-Boc-2-(2-chlorophenyl)-2-hydroxyethanamine
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Synonyms | 2-(Boc-amino)-1-(2-chlorophenyl)ethanol BOC-2-HYDROXY-2-(2-CHLOROPHENYL)-ETHYLAMINE N-Boc-2-(2-chlorophenyl)-2-hydroxyethanaMine N-Boc-2-(2-chlorophenyl)-2-hydroxyethanamine [2-(2-chlorophenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester [2-(2-CHLOROPHENYL)-2-HYDROXYETHYL]-CARBAMIC ACID 1,1-DIMETHYLETHYL ESTER Carbamic acid, N-[2-(2-chlorophenyl)-2-hydroxyethyl]-, 1,1-dimethylethyl ester Carbamic acid,[2-(2-chlorophenyl)-2-hydroxyethyl]-,1,1-dimethylethyl ester (9cl) CARBAMIC ACID, [2-(2-CHLOROPHENYL)-2-HYDROXYETHYL]-, 1,1-DIMETHYLETHYL ESTER (9Cl)
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CAS | 209530-20-1
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[2-(2-chlorophenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester - Physico-chemical Properties
Molecular Formula | C13H18ClNO3
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Molar Mass | 271.74 |
Storage Condition | 2-8℃ |
[2-(2-chlorophenyl)-2-hydroxy-ethyl]-carbamic acid tert-butyl ester - Introduction
N-Boc-2-(2-chlorophyll)-2-hydroxyethanamine is an organic compound with the chemical formula C12H17ClNO3. It has the following important properties:
1. Appearance: N-Boc-2-(2-chlorophenyl)-2-hydroxyethanamine is a solid, usually in the form of white crystals or crystalline powder.
2. Stability: It is relatively stable at room temperature, but should avoid contact with strong oxidants and strong acids.
3. Solubility: N-Boc-2-(2-chlorophenyl)-2-hydroxyethanamine has good solubility in organic solvents, such as diethyl ether, methanol and dichloromethane.
One of the main uses of N-Boc-2-(2-chroophenyl)-2-hydroxyethanamine is as an intermediate in organic synthesis. It can be used to prepare compounds with biological activity, such as drugs, pesticides and biomarkers. It can also be used in the synthesis of other organic compounds, such as substituted hydroxyethylamine, amino alcohols, etc.
The method for preparing N-Boc-2-(2-chlorophenyl)-2-hydroxyethanamine is usually through the compound 2-(2-chlorophenyl)-2-Hydroxyethylamine is obtained by reaction with a Boc acylating agent such as Boc2O or Boc2O DMS. The reaction is usually carried out at room temperature and in the presence of a base.
When using N-Boc-2-(2-chlorine henyl)-2-hydroxyethanamine should pay attention to safety matters. It may cause irritation to the eyes, skin and respiratory tract, so wear appropriate safety protective equipment such as gloves, goggles and protective masks during operation. In addition, it should be operated in a well-ventilated place to avoid inhaling its vapor or dust for a long time. If you come into contact with the compound, rinse immediately with plenty of water and seek medical attention.
Last Update:2024-04-09 20:52:54