N-hydroxyH-imidazo[1,2-a]pyridine-6-carboxamidine
N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide
CAS: 885950-24-3
Molecular Formula: C8H8N4O
N-hydroxyH-imidazo[1,2-a]pyridine-6-carboxamidine - Names and Identifiers
| Name | N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide |
| Synonyms | N'-hydroxy-6-imidazo[2,1-f]pyridinecarboxamidine N'-hydroxyimidazo[2,1-f]pyridine-6-carboxamidine N-hydroxyH-imidazo[1,2-a]pyridine-6-carboxamidine N'-HYDROXYIMIDAZO[1,2-A]PYRIDINE-6-CARBOXIMIDAMIDE N'-hydroxyimidazo[2,1-f]pyridine-6-carboximidamide N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide, N'-Hydroxyimidazo[1,2-a]pyridine-6-carboxamidine |
| CAS | 885950-24-3 |
N-hydroxyH-imidazo[1,2-a]pyridine-6-carboxamidine - Physico-chemical Properties
| Molecular Formula | C8H8N4O |
| Molar Mass | 176.18 |
| Density | 1.48±0.1 g/cm3(Predicted) |
| Melting Point | 191-193 |
| pKa | 10.41±0.50(Predicted) |
| Storage Condition | Room Temprature |
| Sensitive | IRRITANT |
| MDL | MFCD07366550 |
N-hydroxyH-imidazo[1,2-a]pyridine-6-carboxamidine - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Class | IRRITANT |
N-hydroxyH-imidazo[1,2-a]pyridine-6-carboxamidine - Introduction
N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide is an organic compound with the formula C7H8N6O, which is substituted on the imidazole and pyridine rings.
N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide is a white crystalline solid at room temperature, slightly soluble in water, and soluble in acidic and alkaline solutions. It is a molecule with a neutral ring-forming group and has high chemical stability.
The N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide has a variety of applications in the medical field. It is useful as a pharmaceutical intermediate, for example for the synthesis of antitumor and antiviral drugs. In addition, it can also be used as a chemical reagent and catalyst.
The method for preparing N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide can be completed by synthesizing the imidazo[1,2-a]pyridine ring and the hydroxyformamidine group and performing the reaction. The specific preparation method can refer to the relevant chemical literature and patents.
With regard to safety information, the toxicity and hazards associated with N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide have not been clearly reported. However, as an organic compound, appropriate safety measures should be taken when handling and using, avoid direct contact with skin and eyes, and operate under well-ventilated conditions. In case of accidental inhalation or ingestion, seek medical attention immediately. When using this compound, it is best to refer to the relevant safety data sheet and operating manual, and follow laboratory regulations.
N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide is a white crystalline solid at room temperature, slightly soluble in water, and soluble in acidic and alkaline solutions. It is a molecule with a neutral ring-forming group and has high chemical stability.
The N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide has a variety of applications in the medical field. It is useful as a pharmaceutical intermediate, for example for the synthesis of antitumor and antiviral drugs. In addition, it can also be used as a chemical reagent and catalyst.
The method for preparing N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide can be completed by synthesizing the imidazo[1,2-a]pyridine ring and the hydroxyformamidine group and performing the reaction. The specific preparation method can refer to the relevant chemical literature and patents.
With regard to safety information, the toxicity and hazards associated with N'-Hydroxyimidazo[1,2-a]pyridine-6-carboximidamide have not been clearly reported. However, as an organic compound, appropriate safety measures should be taken when handling and using, avoid direct contact with skin and eyes, and operate under well-ventilated conditions. In case of accidental inhalation or ingestion, seek medical attention immediately. When using this compound, it is best to refer to the relevant safety data sheet and operating manual, and follow laboratory regulations.
Last Update：2024-04-09 21:32:52
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