Carbamic acid, N-[(1S)-1-phenylethyl]-, ethyl ester
(S) (-)-ALPHA-PHENETHYLURETHANE
CAS: 33290-12-9
Molecular Formula: C11H15NO2
Carbamic acid, N-[(1S)-1-phenylethyl]-, ethyl ester - Names and Identifiers
| Name | (S) (-)-ALPHA-PHENETHYLURETHANE |
| Synonyms | (S) (-)-ALPHA-PHENETHYLURETHANE Ethyl (S)-1-PhenylethylcarbaMate Carbamic acid, N-[(1S)-1-phenylethyl]-, ethyl ester |
| CAS | 33290-12-9 |
Carbamic acid, N-[(1S)-1-phenylethyl]-, ethyl ester - Physico-chemical Properties
| Molecular Formula | C11H15NO2 |
| Molar Mass | 193.24 |
| Storage Condition | Room Temprature |
Carbamic acid, N-[(1S)-1-phenylethyl]-, ethyl ester - Upstream Downstream Industry
| Downstream Products | (S)-(-)-N,ALPHA-DIMETHYLBENZYLAMINE |
Carbamic acid, N-[(1S)-1-phenylethyl]-, ethyl ester - Introduction
(S) (-)-ALPHA-PHENETHYLURETHANE, also known as (S) (-)-ALPHA-PHENETHYLURETHANE, is an organic compound. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
(S) (-)-ALPHA-PHENETHYLURETHANE is a colorless to pale yellow solid, relatively stable at room temperature. It has an aroma and is soluble in ethanol and ether.
Use:
(S) (-)-ALPHA-PHENETHYLURETHANE is widely used in the field of organic synthesis. It can be used as a chiral catalyst for organic synthesis reactions, especially asymmetric hydrogenation reactions. In addition, it can also be used as an intermediate in the synthesis of other compounds.
Method:
(S) (-)-ALPHA-PHENETHYLURETHANE can be prepared by the following methods: First, phenethyl alcohol and methyl chloroformate are reacted to obtain methyl phenethyl carbamate. The methyl phenethyl carbamate is then separated using an acidic ion exchange resin to give the enantiomerically pure (S) (-)-ALPHA-PHENETHYLURETHANE.
Safety Information:
(S) (-)-The ALPHA-PHENETHYLURETHANE is relatively safe under correct use and storage conditions. However, it can be irritating to the eyes and skin, and may have adverse effects on the respiratory and digestive systems. Follow relevant safe operating procedures and take appropriate protective measures, such as wearing chemical protective gloves and goggles. If you come into contact with the compound, wash the affected area with plenty of water and seek medical help.
Nature:
(S) (-)-ALPHA-PHENETHYLURETHANE is a colorless to pale yellow solid, relatively stable at room temperature. It has an aroma and is soluble in ethanol and ether.
Use:
(S) (-)-ALPHA-PHENETHYLURETHANE is widely used in the field of organic synthesis. It can be used as a chiral catalyst for organic synthesis reactions, especially asymmetric hydrogenation reactions. In addition, it can also be used as an intermediate in the synthesis of other compounds.
Method:
(S) (-)-ALPHA-PHENETHYLURETHANE can be prepared by the following methods: First, phenethyl alcohol and methyl chloroformate are reacted to obtain methyl phenethyl carbamate. The methyl phenethyl carbamate is then separated using an acidic ion exchange resin to give the enantiomerically pure (S) (-)-ALPHA-PHENETHYLURETHANE.
Safety Information:
(S) (-)-The ALPHA-PHENETHYLURETHANE is relatively safe under correct use and storage conditions. However, it can be irritating to the eyes and skin, and may have adverse effects on the respiratory and digestive systems. Follow relevant safe operating procedures and take appropriate protective measures, such as wearing chemical protective gloves and goggles. If you come into contact with the compound, wash the affected area with plenty of water and seek medical help.
Last Update：2024-04-09 21:01:54
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Product Name: (S) (-)-ALPHA-PHENETHYLURETHANE Visit Supplier Webpage Request for quotation
CAS: 33290-12-9
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Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 33290-12-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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Downstream Products for Carbamic acid, N-[(1S)-1-phenylethyl]-, ethyl ester