Pyrido[1,2-a]benzimidazole-4-carboxylic acid, 1,3-dimethyl- - Names and Identifiers
Name | 1,3-Dimethyl-benzo[4,5]imidazo-[1,2-a]pyridine-4-carboxylic acid
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Synonyms | AKOS BC-1832 AKOS BBS-00002690 Pyrido[1,2-a]benzimidazole-4-carboxylic acid, 1,3-dimethyl- 1,3-DIMETHYL-BENZO[4,5]IMIDAZO[1,2-A]PYRIDINE-4-CARBOXYLIC ACID 1,3-Dimethyl-benzo[4,5]imidazo-[1,2-a]pyridine-4-carboxylic acid
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CAS | 10326-57-5
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Pyrido[1,2-a]benzimidazole-4-carboxylic acid, 1,3-dimethyl- - Physico-chemical Properties
Molecular Formula | C14H12N2O2
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Molar Mass | 240.26 |
Storage Condition | Room Temprature |
Sensitive | Irritant |
MDL | MFCD00839716 |
Pyrido[1,2-a]benzimidazole-4-carboxylic acid, 1,3-dimethyl- - Risk and Safety
Hazard Symbols | Xi - Irritant
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Hazard Class | IRRITANT |
Pyrido[1,2-a]benzimidazole-4-carboxylic acid, 1,3-dimethyl- - Introduction
1,3-Dimethy1-benzo [4,5]imidazo-[1,2-a]pyridine-4-carboxylic acid is an organic compound with the chemical formula C14H12N2O2. It is a white crystalline solid.
Nature:
1,3-Dimethy1-benzo [4,5]imidazo-[1,2-a]pyridine-4-carboxylic acid is a compound with aromatic properties. It has high thermal stability and can maintain good stability at high temperatures. It is soluble in organic solvents such as ethanol and methylene chloride at normal temperature, but hardly soluble in water.
Use:
1,3-Dimethy1-benzo [4,5]imidazo-[1,2-a]pyridine-4-carboxylic acid has important applications in drug research and synthesis. It is a commonly used heterocyclic skeleton and is widely used in the synthesis of biologically active organic compounds, drug candidates and derivatives of natural products. Its derivatives have a variety of biological activities, such as antibacterial, anti-tumor and anti-inflammatory, so they have attracted wide attention in drug research and development.
Preparation Method:
1,3-Dimethy1-benzo [4,5]imidazo-[1,2-a]pyridine-4-carboxylic acid The preparation method usually involves the synthesis of multi-step reactions, including the reaction of aniline compounds, cyclization reaction and carboxylation reaction. The specific preparation method can be found in the relevant literature, and the design and operation are carried out according to the experimental conditions.
Safety Information:
Last Update:2024-04-09 02:00:56