1018565-99-5
3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid
CAS: 1018565-99-5
Molecular Formula: C11H11NO3
1018565-99-5 - Names and Identifiers
1018565-99-5 - Physico-chemical Properties
| Molecular Formula | C11H11NO3 |
| Molar Mass | 205.21 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD10018451 |
1018565-99-5 - Risk and Safety
| Hazard Class | IRRITANT |
1018565-99-5 - Introduction
3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid (3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid) is an organic compound. Its molecular formula is C11H11NO3 and its relative molecular mass is 205.21g/mol.
It is a solid with a white to off-white crystalline form. This compound is soluble in most common solvents at room temperature. It can form a stable salt in the presence of sodium hydroxide.
3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid is used as an intermediate in organic synthesis, such as drug synthesis and pesticide synthesis in organic synthesis. It can also be used to prepare biologically active compounds, such as natural products containing a quinoline skeleton and potential drug molecules.
The method for preparing 3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid can be completed by reacting the corresponding dihydroquinoline derivative with chloroacetic acid.
Regarding safety information, due to the lack of specific toxicity studies, the toxicological properties and hazards of 3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid are temporarily unknown. However, as with any chemical, routine laboratory safety procedures should be followed and contact with skin, eyes and respiratory tract must be avoided. When using or handling this compound, it is recommended to have appropriate protective equipment, such as laboratory gloves, protective glasses and protective masks.
It is a solid with a white to off-white crystalline form. This compound is soluble in most common solvents at room temperature. It can form a stable salt in the presence of sodium hydroxide.
3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid is used as an intermediate in organic synthesis, such as drug synthesis and pesticide synthesis in organic synthesis. It can also be used to prepare biologically active compounds, such as natural products containing a quinoline skeleton and potential drug molecules.
The method for preparing 3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid can be completed by reacting the corresponding dihydroquinoline derivative with chloroacetic acid.
Regarding safety information, due to the lack of specific toxicity studies, the toxicological properties and hazards of 3,4-Dihydroquinolin-1(2H)-yl(oxo)acetic acid are temporarily unknown. However, as with any chemical, routine laboratory safety procedures should be followed and contact with skin, eyes and respiratory tract must be avoided. When using or handling this compound, it is recommended to have appropriate protective equipment, such as laboratory gloves, protective glasses and protective masks.
Last Update：2024-04-09 20:45:29
