3-Bromo-6-nitroimidazo[1,2-a]pyridine
3-bromo-6-nitroimidazo[1,2-a]pyridine
CAS: 52310-42-6
Molecular Formula: C7H4BrN3O2
3-Bromo-6-nitroimidazo[1,2-a]pyridine - Names and Identifiers
| Name | 3-bromo-6-nitroimidazo[1,2-a]pyridine |
| Synonyms | 3-Bromo-6-nitroimidazo[1,2-a]pyridine 3-bromo-6-nitroimidazo[1,2-a]pyridine IMidazo[1,2-a]pyridine, 3-broMo-6-nitro- |
| CAS | 52310-42-6 |
3-Bromo-6-nitroimidazo[1,2-a]pyridine - Physico-chemical Properties
| Molecular Formula | C7H4BrN3O2 |
| Molar Mass | 242.03 |
| Density | 1.98±0.1 g/cm3(Predicted) |
| Melting Point | 140-142° |
| pKa | 0.74±0.50(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
| Sensitive | Irritant |
| MDL | MFCD13193088 |
3-Bromo-6-nitroimidazo[1,2-a]pyridine - Risk and Safety
| Hazard Class | IRRITANT |
3-Bromo-6-nitroimidazo[1,2-a]pyridine - Introduction
3-bromo-6-nitroimidazo[1,2-a]pyridine is an organic compound, its molecular formula is C7H4BrN3O2. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: is a yellow to orange solid
-melting point: about 160-165 ℃
-Solubility: Soluble in some organic solvents, such as dimethyl imine, dimethylformamide and dichloromethane.
-Stability: Stable at room temperature, but not stable under strong acid or strong alkali conditions.
Use:
-Chemical research: In organic synthesis, 3-bromo-6-nitroimidazo[1,2-a]pyridine can be used as a starting material, intermediate or reagent.
-Drug research: The compound has potential pharmaceutical activity and may be used to develop antibacterial agents, anti-tumor drugs, etc.
Preparation Method:
The preparation method of 3-bromo-6-nitroimidazo[1,2-a]pyridine is relatively complicated, and a commonly used synthesis route is achieved by bromination and imidazolylation of nitropyridine. Specific synthesis conditions and procedures can be referred to in the specific literature.
Safety Information:
-When using the compound in a laboratory environment, take care to wear appropriate personal protective equipment, such as lab gloves, goggles and protective clothing.
-Due to its potential allergenic and toxic properties, it should be handled with caution and the waste generated should be disposed of properly.
-Avoid contact with strong acids, alkalis and oxidants during handling and storage to prevent accidents.
-This information is only general advice. Specific safety procedures and risk assessments need to refer to the laboratory's safety guidelines and MSDS (chemical safety data sheets).
Nature:
-Appearance: is a yellow to orange solid
-melting point: about 160-165 ℃
-Solubility: Soluble in some organic solvents, such as dimethyl imine, dimethylformamide and dichloromethane.
-Stability: Stable at room temperature, but not stable under strong acid or strong alkali conditions.
Use:
-Chemical research: In organic synthesis, 3-bromo-6-nitroimidazo[1,2-a]pyridine can be used as a starting material, intermediate or reagent.
-Drug research: The compound has potential pharmaceutical activity and may be used to develop antibacterial agents, anti-tumor drugs, etc.
Preparation Method:
The preparation method of 3-bromo-6-nitroimidazo[1,2-a]pyridine is relatively complicated, and a commonly used synthesis route is achieved by bromination and imidazolylation of nitropyridine. Specific synthesis conditions and procedures can be referred to in the specific literature.
Safety Information:
-When using the compound in a laboratory environment, take care to wear appropriate personal protective equipment, such as lab gloves, goggles and protective clothing.
-Due to its potential allergenic and toxic properties, it should be handled with caution and the waste generated should be disposed of properly.
-Avoid contact with strong acids, alkalis and oxidants during handling and storage to prevent accidents.
-This information is only general advice. Specific safety procedures and risk assessments need to refer to the laboratory's safety guidelines and MSDS (chemical safety data sheets).
Last Update：2024-04-09 21:04:16
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