92976-98-2
(S)-1,2,3,4-Tetrahydro-Quinoline-2-Carboxylic Acid
CAS: 92976-98-2
Molecular Formula: C10H11NO2
92976-98-2 - Names and Identifiers
92976-98-2 - Physico-chemical Properties
| Molecular Formula | C10H11NO2 |
| Molar Mass | 177.2 |
92976-98-2 - Risk and Safety
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. |
92976-98-2 - Introduction
(S)-1,2,3, Acid is an organic compound with the chemical formula C11H13NO2. It is a white crystalline solid, soluble in polar solvents such as ethanol and dimethylformamide.
(S)-1,2,3, Acid has important applications in the field of drug synthesis and medicine. It is a chiral molecule and can play an important role as a chiral inducer in the optical separation process of synthetic drugs. In addition, it can also be used for the preparation of quinoline compounds, such as antidepressants, antipsychotics, etc.
The method of preparing (S)-1,2,3, Acid is usually obtained by chiral separation of quinoline compounds. The specific preparation process may vary depending on the specific synthetic route, but generally chiral separation techniques (such as chiral polymers, chiral chromatography, etc.) are used to obtain pure (S)-1,2,3, Acid.
Care should be taken in the use and storage of (S)-1,2,3, Acid. It may be irritating to the eyes, skin and respiratory system. Contact should be avoided and personal protective measures should be taken. In addition, it should be stored in a dry, well-ventilated place, and away from flammable materials and oxidants. Specific safety information should be evaluated based on the specific substance quality and use. In the use and operation, should follow the relevant safety procedures and standards.
(S)-1,2,3, Acid has important applications in the field of drug synthesis and medicine. It is a chiral molecule and can play an important role as a chiral inducer in the optical separation process of synthetic drugs. In addition, it can also be used for the preparation of quinoline compounds, such as antidepressants, antipsychotics, etc.
The method of preparing (S)-1,2,3, Acid is usually obtained by chiral separation of quinoline compounds. The specific preparation process may vary depending on the specific synthetic route, but generally chiral separation techniques (such as chiral polymers, chiral chromatography, etc.) are used to obtain pure (S)-1,2,3, Acid.
Care should be taken in the use and storage of (S)-1,2,3, Acid. It may be irritating to the eyes, skin and respiratory system. Contact should be avoided and personal protective measures should be taken. In addition, it should be stored in a dry, well-ventilated place, and away from flammable materials and oxidants. Specific safety information should be evaluated based on the specific substance quality and use. In the use and operation, should follow the relevant safety procedures and standards.
Last Update：2024-04-09 20:52:54
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View History
92976-98-2
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53014-84-9
552-37-4
calcium dithiocyanate
78-36-4
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lepuron
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10166-08-2
Ixazomib Impurity 63