1146118-69-5
3-Ethyl-4-fluoro-1H-indazole
CAS: 1146118-69-5
Molecular Formula: C9H9FN2
1146118-69-5 - Names and Identifiers
| Name | 3-Ethyl-4-fluoro-1H-indazole |
| Synonyms | 3-Ethyl-4-fluoro-1H-indazole 1H-Indazole, 3-ethyl-4-fluoro- |
| CAS | 1146118-69-5 |
| InChI | InChI=1S/C9H9FN2/c1-2-7-9-6(10)4-3-5-8(9)12-11-7/h3-5H,2H2,1H3,(H,11,12) |
1146118-69-5 - Physico-chemical Properties
| Molecular Formula | C9H9FN2 |
| Molar Mass | 164.18 |
1146118-69-5 - Introduction
3-Ethyl-4-fluoroindazole is an organic compound with the chemical formula C7H8FN2.
Nature:
3-Ethyl-4-fluoroindazole is a white crystalline solid that is stable at room temperature. It has low solubility in water, but can be dissolved in many organic solvents. It has a strong odor.
Use:
3-Ethyl-4-fluoroindazole has a wide range of applications in the field of medicine. It is an important intermediate compound for the synthesis of various drugs and medical compounds. It can be used as a raw material for antibiotics, anticancer drugs and antiviral drugs.
Method:
The preparation methods of 3-ethyl-4-fluoroindazole are more diversified. A common method is to react 3-ethylindazole with hydrogen fluoride under acidic conditions to obtain the desired product.
Safety Information:
3-Ethyl-4-fluoroindazole is safer for humans and the environment under normal conditions of use. However, like all chemicals, it still carries some risks. Use should comply with relevant operating procedures and safety measures, including wearing appropriate protective equipment and operating in a well-ventilated area.
Nature:
3-Ethyl-4-fluoroindazole is a white crystalline solid that is stable at room temperature. It has low solubility in water, but can be dissolved in many organic solvents. It has a strong odor.
Use:
3-Ethyl-4-fluoroindazole has a wide range of applications in the field of medicine. It is an important intermediate compound for the synthesis of various drugs and medical compounds. It can be used as a raw material for antibiotics, anticancer drugs and antiviral drugs.
Method:
The preparation methods of 3-ethyl-4-fluoroindazole are more diversified. A common method is to react 3-ethylindazole with hydrogen fluoride under acidic conditions to obtain the desired product.
Safety Information:
3-Ethyl-4-fluoroindazole is safer for humans and the environment under normal conditions of use. However, like all chemicals, it still carries some risks. Use should comply with relevant operating procedures and safety measures, including wearing appropriate protective equipment and operating in a well-ventilated area.
Last Update：2024-04-09 20:45:29
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