2-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-, methyl ester, (2S)-
methyl (2S)-1,2,3,4-tetrahydroquinoline-2-carboxylate
CAS: 63492-82-0
Molecular Formula: C11H13NO2
2-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-, methyl ester, (2S)- - Names and Identifiers
2-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-, methyl ester, (2S)- - Physico-chemical Properties
| Molecular Formula | C11H13NO2 |
| Molar Mass | 191.23 |
| Density | 1.125±0.06 g/cm3(Predicted) |
| Boling Point | 315.0±31.0 °C(Predicted) |
| Flash Point | 144.3°C |
| Vapor Presure | 0.000449mmHg at 25°C |
| pKa | 3.08±0.40(Predicted) |
| Refractive Index | 1.532 |
2-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-, methyl ester, (2S)- - Risk and Safety
| Hazard Symbols | T - Toxic |
| Risk Codes | 25 - Toxic if swallowed |
| Safety Description | 45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
2-Quinolinecarboxylic acid, 1,2,3,4-tetrahydro-, methyl ester, (2S)- - Introduction
methyl (2S)-1,2,3, is an organic compound. Its chemical formula is C12H15NO2 and its molecular weight is 205.25g/mol.
This compound is a colorless liquid with a peculiar odor. It is insoluble in water at room temperature and soluble in organic solvents such as alcohols and ethers. It has chirality, specifically the (S)-enantiomer. Its optical rotation is 5.5 °.
methyl (2S)-1,2,3, has important applications in organic synthesis. It is often used as a raw material for chiral catalysts for the synthesis of chiral drugs and compounds. In addition, it can also be used as dyes and organic synthesis intermediates.
The method for preparing methyl (2S)-1,2,3, phenyl is generally obtained by chiral reduction of quinoline. As a specific production method, the reaction can be carried out under appropriate temperature and pH conditions using a suspended reducing agent or a metal catalyst.
Regarding safety information, the toxicity of this compound is low, but as an organic compound, it is still necessary to pay attention to safe operation. When touching skin or inhaling, avoid prolonged exposure or direct contact, and use personal protective equipment if necessary. When used in a laboratory environment, the safe handling procedures and relevant regulations for chemicals should be observed.
This compound is a colorless liquid with a peculiar odor. It is insoluble in water at room temperature and soluble in organic solvents such as alcohols and ethers. It has chirality, specifically the (S)-enantiomer. Its optical rotation is 5.5 °.
methyl (2S)-1,2,3, has important applications in organic synthesis. It is often used as a raw material for chiral catalysts for the synthesis of chiral drugs and compounds. In addition, it can also be used as dyes and organic synthesis intermediates.
The method for preparing methyl (2S)-1,2,3, phenyl is generally obtained by chiral reduction of quinoline. As a specific production method, the reaction can be carried out under appropriate temperature and pH conditions using a suspended reducing agent or a metal catalyst.
Regarding safety information, the toxicity of this compound is low, but as an organic compound, it is still necessary to pay attention to safe operation. When touching skin or inhaling, avoid prolonged exposure or direct contact, and use personal protective equipment if necessary. When used in a laboratory environment, the safe handling procedures and relevant regulations for chemicals should be observed.
Last Update：2024-04-09 20:52:54
Supplier List
View History