(S)-tert-Butyl (1-(3-chlorophenyl)-2-hydroxyethyl)carbamate
Carbamic acid, N-[(1S)-1-(3-chlorophenyl)-2-hydroxyethyl]-, 1,1-dimethylethyl ester
CAS: 1379546-46-9
Molecular Formula: C13H18ClNO3
(S)-tert-Butyl (1-(3-chlorophenyl)-2-hydroxyethyl)carbamate - Names and Identifiers
(S)-tert-Butyl (1-(3-chlorophenyl)-2-hydroxyethyl)carbamate - Physico-chemical Properties
| Molecular Formula | C13H18ClNO3 |
| Molar Mass | 271.74 |
| Storage Condition | 2-8°C |
(S)-tert-Butyl (1-(3-chlorophenyl)-2-hydroxyethyl)carbamate - Introduction
(S)-B-(Boc-amino)-3-chlorophenethanol is an organic compound with the following properties:
1. Appearance: white crystalline solid
2. molecular formula: C13H17ClNO3
3. Molecular weight: 271.7g/mol
Use of (S)-B-(Boc-amino)-3-chlorophenylethyl alcohol:
This compound is often used in some important reactions in the field of organic synthesis, mainly for the synthesis of biologically active compounds, such as pharmaceutical intermediates and chiral ligands. In addition, it can also be used as a chiral inducer to catalyze asymmetric reactions.
Preparation Method:
The preparation method of (S)-B-(Boc-amino)-3-chlorophenethanol is as follows:
First, (3-chlorophenyl)-[(1,1-dimethylethylamino) (amino) methyl]-methanol is reacted with N-tert-butoxycarbonyl oxime in an appropriate solvent to obtain a double bond ketone, and then the double bond ketone is reduced to (S)-B-(Boc-amino)-3-chlorophenethanol by a reduction reaction.
Safety Information:
During operation, it is necessary to pay attention to the toxicity and irritation of the compound, and appropriate protective equipment should be worn to avoid contact with skin and eyes. At the same time, it is necessary to operate in a well-ventilated place to avoid inhaling aerosol-like substances. If ingestion or skin contact occurs, seek medical attention immediately and bring the compound's safety data sheet with you.
1. Appearance: white crystalline solid
2. molecular formula: C13H17ClNO3
3. Molecular weight: 271.7g/mol
Use of (S)-B-(Boc-amino)-3-chlorophenylethyl alcohol:
This compound is often used in some important reactions in the field of organic synthesis, mainly for the synthesis of biologically active compounds, such as pharmaceutical intermediates and chiral ligands. In addition, it can also be used as a chiral inducer to catalyze asymmetric reactions.
Preparation Method:
The preparation method of (S)-B-(Boc-amino)-3-chlorophenethanol is as follows:
First, (3-chlorophenyl)-[(1,1-dimethylethylamino) (amino) methyl]-methanol is reacted with N-tert-butoxycarbonyl oxime in an appropriate solvent to obtain a double bond ketone, and then the double bond ketone is reduced to (S)-B-(Boc-amino)-3-chlorophenethanol by a reduction reaction.
Safety Information:
During operation, it is necessary to pay attention to the toxicity and irritation of the compound, and appropriate protective equipment should be worn to avoid contact with skin and eyes. At the same time, it is necessary to operate in a well-ventilated place to avoid inhaling aerosol-like substances. If ingestion or skin contact occurs, seek medical attention immediately and bring the compound's safety data sheet with you.
Last Update：2024-04-09 21:11:58
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CAS: 1379546-46-9
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Product Name: CarbaMic acid, N-[(1S)-1-(3-chlorophenyl)-2-hydroxyethyl]-, 1,1-diMethylethyl ester Visit Supplier Webpage Request for quotation
CAS: 1379546-46-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 1379546-46-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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