(S)-2-Dimethylamino-1-phenyletanol
(S)-2-Dimethylamino-1-phenyletanol
CAS: 2202-69-9
Molecular Formula: C10H15NO
(S)-2-Dimethylamino-1-phenyletanol - Names and Identifiers
(S)-2-Dimethylamino-1-phenyletanol - Physico-chemical Properties
| Molecular Formula | C10H15NO |
| Molar Mass | 165.23 |
| Density | 1.027±0.06 g/cm3(Predicted) |
| Boling Point | 85-90 °C(Press: 3-4 Torr) |
| pKa | 14.06±0.20(Predicted) |
| Use | Use (S)-2-dimethylamino-1-phenylethanol is an alcoholic organic substance, which can be used as a pharmaceutical intermediate. |
(S)-2-Dimethylamino-1-phenyletanol - Introduction
(S)-is an organic compound with the chemical formula C10H15NO. It is solid at room temperature and soluble in water and organic solvents.
This compound has chirality, and there are two enantiomers (S) and (R). Specific to (S)-, it is an organic base that can be used as a catalyst or reagent and is widely used in organic synthesis reactions.
Its Main uses include catalyzing and promoting asymmetric synthesis reactions, such as asymmetric reduction, asymmetric rearrangement and asymmetric nucleophilic substitution. By selecting appropriate catalysts and reaction conditions, compounds with high Stereoselectivity can be efficiently synthesized.
The preparation method of
(S)-is generally obtained by partial reduction of (dimethylamino) acetophenone. Common reducing agents include metal hydrides such as lithium aluminum hydride (LiAlH4) or mercapto borates (CBS) and the like.
Regarding safety information, this compound is an organic compound that is irritating to the skin, eyes and respiratory tract and should be worn with appropriate protective equipment. During handling and use, safe operating procedures should be observed and adequate ventilation should be ensured. In addition, it may be toxic to aquatic organisms, and waste and wastewater should be properly disposed. Please pay attention to safety during use.
This compound has chirality, and there are two enantiomers (S) and (R). Specific to (S)-, it is an organic base that can be used as a catalyst or reagent and is widely used in organic synthesis reactions.
Its Main uses include catalyzing and promoting asymmetric synthesis reactions, such as asymmetric reduction, asymmetric rearrangement and asymmetric nucleophilic substitution. By selecting appropriate catalysts and reaction conditions, compounds with high Stereoselectivity can be efficiently synthesized.
The preparation method of
(S)-is generally obtained by partial reduction of (dimethylamino) acetophenone. Common reducing agents include metal hydrides such as lithium aluminum hydride (LiAlH4) or mercapto borates (CBS) and the like.
Regarding safety information, this compound is an organic compound that is irritating to the skin, eyes and respiratory tract and should be worn with appropriate protective equipment. During handling and use, safe operating procedures should be observed and adequate ventilation should be ensured. In addition, it may be toxic to aquatic organisms, and waste and wastewater should be properly disposed. Please pay attention to safety during use.
Last Update：2024-04-10 22:29:15
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Product Name: (S)-2-Dimethylamino-1-phenyletanol, GC 97% Request for quotation
CAS: 2202-69-9
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Product Name: (S)-2-Dimethylamino-1-phenyletanol, GC 97% Visit Supplier Webpage Request for quotation
CAS: 2202-69-9
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Email: 3008007409@qq.com
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QQ: 3008007409
CAS: 2202-69-9
Tel: 18301782025
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View History
(S)-2-Dimethylamino-1-phenyletanol
1456877-72-7
1-(7-AMINO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)ETHANONE
128676-85-7
6473-13-8
33471-40-8
56092-81-0
25013-15-4
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Agmatine dihydrochloride
1456877-72-7
1-(7-AMINO-2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)ETHANONE
128676-85-7
6473-13-8
33471-40-8
56092-81-0
25013-15-4
7-Fluoronaphthalen-1-ol
Agmatine dihydrochloride