4-(4-aMino-2-fluorophenoxy)-picolinaMide
4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide
CAS: 868733-71-5
Molecular Formula: C12H10FN3O2
4-(4-aMino-2-fluorophenoxy)-picolinaMide - Names and Identifiers
| Name | 4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide |
| Synonyms | 4-(4-amino-2-fluorophenoxy)-picolinamide 4-(4-aMino-2-fluorophenoxy)-picolinaMide 4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide |
| CAS | 868733-71-5 |
| InChI | InChI=1/C12H10FN3O2/c13-9-5-7(14)1-2-11(9)18-8-3-4-16-10(6-8)12(15)17/h1-6H,14H2,(H2,15,17) |
4-(4-aMino-2-fluorophenoxy)-picolinaMide - Physico-chemical Properties
| Molecular Formula | C12H10FN3O2 |
| Molar Mass | 247.23 |
| Density | 1.385g/cm3 |
| Boling Point | 440.6°C at 760 mmHg |
| Flash Point | 220.3°C |
| Vapor Presure | 5.82E-08mmHg at 25°C |
| Refractive Index | 1.635 |
4-(4-aMino-2-fluorophenoxy)-picolinaMide - Introduction
4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide is a compound whose chemical formula is C12H9FN2O2. It is a colorless to pale yellow solid.
This compound has a wide range of applications in many fields. One of its main uses is as an intermediate in organic synthesis. It can be used to synthesize drugs and pesticides containing pyridine structures, which play an important role in the regulation of biological activity.
There are many methods for preparing 4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide, one of which is synthesis by substitution reaction. In general, 4-amino-2-fluorophenol is reacted with pyridine-2-carboxylic anhydride under appropriate conditions to give the desired product.
You need to pay attention to safety when using and handling 4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide. It may be irritating to the eyes, skin and respiratory system, so protective equipment should be worn during operation. In addition, it may also be harmful to the environment and should be avoided. It needs to be properly managed during use and storage and to comply with relevant safe operating procedures.
This compound has a wide range of applications in many fields. One of its main uses is as an intermediate in organic synthesis. It can be used to synthesize drugs and pesticides containing pyridine structures, which play an important role in the regulation of biological activity.
There are many methods for preparing 4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide, one of which is synthesis by substitution reaction. In general, 4-amino-2-fluorophenol is reacted with pyridine-2-carboxylic anhydride under appropriate conditions to give the desired product.
You need to pay attention to safety when using and handling 4-(4-amino-2-fluorophenoxy)pyridine-2-carboxamide. It may be irritating to the eyes, skin and respiratory system, so protective equipment should be worn during operation. In addition, it may also be harmful to the environment and should be avoided. It needs to be properly managed during use and storage and to comply with relevant safe operating procedures.
Last Update：2024-04-09 20:52:54
