1226808-60-1
2-(2-(4-Bromo-1H-pyrazol-1-yl)-ethyl)isoindoline-1,3-dione
CAS: 1226808-60-1
Molecular Formula: C13H10BrN3O2
1226808-60-1 - Names and Identifiers
1226808-60-1 - Physico-chemical Properties
| Molecular Formula | C13H10BrN3O2 |
| Molar Mass | 320.14 |
| Storage Condition | Room temperature. |
| Sensitive | IRRITANT |
| MDL | MFCD16295091 |
1226808-60-1 - Introduction
2-(2-(isoindoline-1)-ethyl, 3-dione is an organic compound with the chemical formula C15H10BrN3O2. The following is an introduction to its nature, use, preparation and safety information:
Nature:
2-(2-)-ethyl isoindoline-1,3-dione is a yellow solid. It is an organohalogen compound with bromine and pyrazole groups. It is stable at room temperature, but should avoid direct sunlight.
Use:
2-(2-(over)-ethyl)isoindoline-1,3-dione is often used as an intermediate in organic synthesis. It can be used to synthesize other compounds, such as drugs, pesticides and dyes. This compound has certain antibacterial, anti-inflammatory and biological activities, so it also has potential application value in the field of drug research.
Preparation Method:
2-(2-(over)-ethyl)isoindoline-1,3-dione can be synthesized by a variety of methods, the following is a brief step of a synthesis method:
1.2-(4-bromopyrazol-1-yl) ethanamine reacts with phthalimide to generate 2-(2-(4-bromopyrazol-1-yl) isoindoline-1, the intermediate of 3-dione.
2. carry out corresponding reaction purification and purification process steps, such as crystallization, removal of reaction solvent, etc.
3. Finally, 2-(2-(Al)-ethyl)isoindoline-1,3-dione, was obtained, and crystallized or dried to obtain a pure product.
Safety Information:
2-(2-)-ethyl isoindoline-1,3-dione has no obvious toxicity under normal operating conditions. However, like all organic bromine compounds, it is somewhat irritating and corrosive. Use should wear appropriate protective equipment to avoid direct contact with skin and eyes. At the same time, it should be operated in a well-ventilated place to avoid inhaling its odor and generating harmful vapors. When handling this compound, follow safe practices and dispose of waste properly. In case of any accident, corresponding first aid measures shall be taken immediately. During storage, keep it sealed and away from ignition, high temperature and oxidizing agents.
Nature:
2-(2-)-ethyl isoindoline-1,3-dione is a yellow solid. It is an organohalogen compound with bromine and pyrazole groups. It is stable at room temperature, but should avoid direct sunlight.
Use:
2-(2-(over)-ethyl)isoindoline-1,3-dione is often used as an intermediate in organic synthesis. It can be used to synthesize other compounds, such as drugs, pesticides and dyes. This compound has certain antibacterial, anti-inflammatory and biological activities, so it also has potential application value in the field of drug research.
Preparation Method:
2-(2-(over)-ethyl)isoindoline-1,3-dione can be synthesized by a variety of methods, the following is a brief step of a synthesis method:
1.2-(4-bromopyrazol-1-yl) ethanamine reacts with phthalimide to generate 2-(2-(4-bromopyrazol-1-yl) isoindoline-1, the intermediate of 3-dione.
2. carry out corresponding reaction purification and purification process steps, such as crystallization, removal of reaction solvent, etc.
3. Finally, 2-(2-(Al)-ethyl)isoindoline-1,3-dione, was obtained, and crystallized or dried to obtain a pure product.
Safety Information:
2-(2-)-ethyl isoindoline-1,3-dione has no obvious toxicity under normal operating conditions. However, like all organic bromine compounds, it is somewhat irritating and corrosive. Use should wear appropriate protective equipment to avoid direct contact with skin and eyes. At the same time, it should be operated in a well-ventilated place to avoid inhaling its odor and generating harmful vapors. When handling this compound, follow safe practices and dispose of waste properly. In case of any accident, corresponding first aid measures shall be taken immediately. During storage, keep it sealed and away from ignition, high temperature and oxidizing agents.
Last Update：2024-04-09 21:11:58
