(S)-4-(1-AMinoethyl)benzonitrile
(S)-(-)-1-(4-Cyanophenyl)ethylamine
CAS: 36244-70-9
Molecular Formula: C9H10N2
(S)-4-(1-AMinoethyl)benzonitrile - Names and Identifiers
(S)-4-(1-AMinoethyl)benzonitrile - Physico-chemical Properties
| Molecular Formula | C9H10N2 |
| Molar Mass | 146.19 |
| Density | 1.06±0.1 g/cm3(Predicted) |
| Boling Point | 273.7±23.0 °C(Predicted) |
| pKa | 8.42±0.10(Predicted) |
| Storage Condition | 2-8°C |
(S)-4-(1-AMinoethyl)benzonitrile - Introduction
(S)-(-)-1-(4-Cyanophenyl)ethylamine is a chiral organic compound with the chemical formula C10H10N2. It exists in the solid state as colorless crystals or powder.
The molecular structure of the (S)-(-)-1-(4-Cyanophenyl)ethylamine contains a chiral center, so it has two enantiomers, namely (S)-and (R)-two stereoisomers. It is an amino alkane compound with weak alkalinity.
In practical applications,(S)-(-)-1-(4-Cyanophenyl)ethylamine are widely used in synthetic reactions and organic synthesis in the pharmaceutical industry. It is often used as an intermediate in drug synthesis and can be used to synthesize biologically active compounds, such as drugs and biologically active molecules.
The preparation method of (S)-(-)-1-(4-Cyanophenyl)ethylamine is relatively simple. A commonly used method is to synthesize by reducing aromatic amines. In particular, p-aminobenzoic acid can be reacted with sodium cyanide under the action of a reducing agent to give the corresponding product.
Regarding safety information, since this compound is an organic compound and has strong chemical reaction activity, safety measures should be paid attention to during operation. It is also necessary to properly store and dispose of the waste of the compound and follow the relevant safety procedures. Appropriate personal protective equipment, such as chemical gloves, goggles and laboratory coats, should be used during use. Before operating, it is recommended to understand and follow the relevant safe operation guidelines in detail.
The molecular structure of the (S)-(-)-1-(4-Cyanophenyl)ethylamine contains a chiral center, so it has two enantiomers, namely (S)-and (R)-two stereoisomers. It is an amino alkane compound with weak alkalinity.
In practical applications,(S)-(-)-1-(4-Cyanophenyl)ethylamine are widely used in synthetic reactions and organic synthesis in the pharmaceutical industry. It is often used as an intermediate in drug synthesis and can be used to synthesize biologically active compounds, such as drugs and biologically active molecules.
The preparation method of (S)-(-)-1-(4-Cyanophenyl)ethylamine is relatively simple. A commonly used method is to synthesize by reducing aromatic amines. In particular, p-aminobenzoic acid can be reacted with sodium cyanide under the action of a reducing agent to give the corresponding product.
Regarding safety information, since this compound is an organic compound and has strong chemical reaction activity, safety measures should be paid attention to during operation. It is also necessary to properly store and dispose of the waste of the compound and follow the relevant safety procedures. Appropriate personal protective equipment, such as chemical gloves, goggles and laboratory coats, should be used during use. Before operating, it is recommended to understand and follow the relevant safe operation guidelines in detail.
Last Update：2024-04-09 21:54:55
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View History
(S)-4-(1-AMinoethyl)benzonitrile
2-羟基-1,2,3-丙烷三甲酸锌盐
3-丁烯-2-醇
(2,4-二甲基噻唑-5)-甲醇
1-(4-isopropylphenyl)hydrazine hydrochloride
2-(6-甲氧基萘-1-基)丙烷-1,3-二醇
1-FLUORO-2-NITRO-4-(TRIFLUOROMETHYL)BENZENE
2-羟基-1,2,3-丙烷三甲酸锌盐
3-丁烯-2-醇
(2,4-二甲基噻唑-5)-甲醇
1-(4-isopropylphenyl)hydrazine hydrochloride
2-(6-甲氧基萘-1-基)丙烷-1,3-二醇
1-FLUORO-2-NITRO-4-(TRIFLUOROMETHYL)BENZENE