1H-Imidazol-2-carboxamide
1H-Imidazol-2-carboxamide
CAS: 16093-82-6
Molecular Formula: C4H5N3O
1H-Imidazol-2-carboxamide - Names and Identifiers
| Name | 1H-Imidazol-2-carboxamide |
| Synonyms | 1H-Imidazol-2-carboxamide 1H-Imidazole-2-carboxamide |
| CAS | 16093-82-6 |
| InChI | InChI=1/C4H5N3O/c5-3(8)4-6-1-2-7-4/h1-2H,(H2,5,8)(H,6,7) |
1H-Imidazol-2-carboxamide - Physico-chemical Properties
| Molecular Formula | C4H5N3O |
| Molar Mass | 111.1 |
| Density | 1.394±0.06 g/cm3(Predicted) |
| Melting Point | 312-313 °C (decomp) |
| Boling Point | 365.4±25.0 °C(Predicted) |
| Flash Point | 174.8°C |
| Vapor Presure | 1.58E-05mmHg at 25°C |
| pKa | 11.61±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.612 |
1H-Imidazol-2-carboxamide - Introduction
1H-Imidazol-2-carboxamide is an organic compound with the chemical formula C4H5N3O. It is a colorless to light yellow solid, stable at room temperature.
1H-Imidazol-2-carboxamide has good solubility and is soluble in water, alcohols and ketones. It is a weak base that reacts with acids to form salts. In addition, 1H-Imidazol-2-carboxamide has good stability and has a certain tolerance to oxidants and acid-base environments.
1H-Imidazol-2-carboxamide has a wide range of applications. It can be used as a solvent for organic synthesis reactions, especially for catalysts and enzyme-catalyzed reactions. In addition, 1H-Imidazol-2-carboxamide can also be used as intermediates in certain organic synthesis reactions, such as the synthesis of active substances in the field of pesticides and pharmaceuticals.
The preparation method of 1H-Imidazol-2-carboxamide is mainly obtained by the reaction of imidazole and formyl chloride. In the reaction, imidazole is dissolved in an organic solvent and then formyl chloride is added to give 1H-Imidazol-2-carboxamide. The reaction conditions are generally carried out at room temperature, and the molar ratio of the reactants can be adjusted as needed.
Pay attention to safety when using 1H-Imidazol-2-carboxamide. It is an organic compound and should avoid direct contact with the skin and eyes, and avoid inhalation or swallowing. Wear appropriate protective equipment such as gloves, goggles and face shields during operation. At the same time, it should be operated in a well-ventilated place to avoid the accumulation of harmful gases.
This information is for reference only, specific use and operation should follow the safety procedures and laboratory guidance.
1H-Imidazol-2-carboxamide has good solubility and is soluble in water, alcohols and ketones. It is a weak base that reacts with acids to form salts. In addition, 1H-Imidazol-2-carboxamide has good stability and has a certain tolerance to oxidants and acid-base environments.
1H-Imidazol-2-carboxamide has a wide range of applications. It can be used as a solvent for organic synthesis reactions, especially for catalysts and enzyme-catalyzed reactions. In addition, 1H-Imidazol-2-carboxamide can also be used as intermediates in certain organic synthesis reactions, such as the synthesis of active substances in the field of pesticides and pharmaceuticals.
The preparation method of 1H-Imidazol-2-carboxamide is mainly obtained by the reaction of imidazole and formyl chloride. In the reaction, imidazole is dissolved in an organic solvent and then formyl chloride is added to give 1H-Imidazol-2-carboxamide. The reaction conditions are generally carried out at room temperature, and the molar ratio of the reactants can be adjusted as needed.
Pay attention to safety when using 1H-Imidazol-2-carboxamide. It is an organic compound and should avoid direct contact with the skin and eyes, and avoid inhalation or swallowing. Wear appropriate protective equipment such as gloves, goggles and face shields during operation. At the same time, it should be operated in a well-ventilated place to avoid the accumulation of harmful gases.
This information is for reference only, specific use and operation should follow the safety procedures and laboratory guidance.
Last Update：2024-04-09 21:11:58
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CAS: 16093-82-6
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QQ: 3008007409
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CAS: 16093-82-6
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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