N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide
N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide
CAS: 1186311-00-1
Molecular Formula: C7H7IN2O2
N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide - Names and Identifiers
| Name | N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide |
| Synonyms | N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide Acetamide, N-(4-hydroxy-5-iodo-3-pyridinyl)- |
| CAS | 1186311-00-1 |
N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide - Physico-chemical Properties
| Molecular Formula | C7H7IN2O2 |
| Molar Mass | 278.05 |
| Density | 2.040±0.06 g/cm3(Predicted) |
| Boling Point | 462.8±45.0 °C(Predicted) |
| pKa | 3.08±0.50(Predicted) |
| Storage Condition | 2-8℃ |
| Sensitive | IRRITANT |
| MDL | MFCD12922751 |
N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide - Risk and Safety
| Hazard Class | IRRITANT |
N-(4-Hydroxy-5-iodopyridin-3-yl)acetamide - Introduction
N-acetamide is an organic compound with the chemical formula C8H8IN2O2.
Nature:
N-(acetamide) is a white crystalline solid. It is stable at room temperature, but may decompose in high temperature or humid environment. It is stable to water and acids, but is susceptible to hydrolysis under alkaline conditions.
Use:
N-(acetamide) is commonly used in organic synthesis. It can be used as a chelating agent, reagent, intermediate and ligand, and participate in a variety of organic reactions, such as the acylation of carbonyl compounds, the carbonylation of alcohols, and the synthesis of heterocyclic compounds. It is also frequently used in the preparation of other organic compounds.
Preparation Method: The preparation of
N-acetamide generally involves a chemical reaction step. The target product can be obtained by adding 5-iodo-4-oxo-1, 4-dihydropyridin-3-one to ammonia, followed by an acylation reaction.
Safety Information:
N-(acetamide) Please refer to the relevant safety data sheet (SDS) for specific safety information. As an organic compound, the use should strictly follow the laboratory safety procedures. Avoid skin contact and inhalation to prevent accidental ingestion. During use and storage, care should be taken to avoid high temperatures, fire sources and humid environments.
Nature:
N-(acetamide) is a white crystalline solid. It is stable at room temperature, but may decompose in high temperature or humid environment. It is stable to water and acids, but is susceptible to hydrolysis under alkaline conditions.
Use:
N-(acetamide) is commonly used in organic synthesis. It can be used as a chelating agent, reagent, intermediate and ligand, and participate in a variety of organic reactions, such as the acylation of carbonyl compounds, the carbonylation of alcohols, and the synthesis of heterocyclic compounds. It is also frequently used in the preparation of other organic compounds.
Preparation Method: The preparation of
N-acetamide generally involves a chemical reaction step. The target product can be obtained by adding 5-iodo-4-oxo-1, 4-dihydropyridin-3-one to ammonia, followed by an acylation reaction.
Safety Information:
N-(acetamide) Please refer to the relevant safety data sheet (SDS) for specific safety information. As an organic compound, the use should strictly follow the laboratory safety procedures. Avoid skin contact and inhalation to prevent accidental ingestion. During use and storage, care should be taken to avoid high temperatures, fire sources and humid environments.
Last Update：2024-04-10 22:29:15
