3-AMINO-4-IMIDAZOL-1-YL-BENZOIC ACID
3-Amino-4-imidazol-1-yl-benzoic acid
CAS: 853743-43-8
Molecular Formula: C10H9N3O2
3-AMINO-4-IMIDAZOL-1-YL-BENZOIC ACID - Names and Identifiers
3-AMINO-4-IMIDAZOL-1-YL-BENZOIC ACID - Physico-chemical Properties
| Molecular Formula | C10H9N3O2 |
| Molar Mass | 203.2 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD06762988 |
3-AMINO-4-IMIDAZOL-1-YL-BENZOIC ACID - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Class | IRRITANT |
3-AMINO-4-IMIDAZOL-1-YL-BENZOIC ACID - Introduction
Kappa (3-amino-4-imidazol-1-ylbenzoic acid) is an organic compound with the chemical formula C10H9N3O2.
Nature:
acid is a white solid, soluble in some organic solvents such as chloroform, methanol and dichloromethane, insoluble in water. It has the chemical properties of oxalic acid.
Use:
Acid has certain application value in the field of medicine. It is a non-classical non-enzyme inhibitor, which can be used for the development of new drugs, especially the research and development of antibacterial drugs.
Preparation Method:
The preparation of anion acid is usually done by synthetic methods. Specifically, the target product can be obtained by reacting benzoyl chloride with Imidazole-1-carboxylic acid, and then adding ammonia water under alkaline conditions to cause amination reaction.
Safety Information:
There is limited information regarding the safety of the. acid. Due to its limited solubility and use, its toxicity and harmfulness have been less studied and evaluated. Regular laboratory safety procedures should be followed in handling and use, and adequate ventilation should be ensured. If necessary, the compound should be used and handled under the guidance of a professional.
Nature:
acid is a white solid, soluble in some organic solvents such as chloroform, methanol and dichloromethane, insoluble in water. It has the chemical properties of oxalic acid.
Use:
Acid has certain application value in the field of medicine. It is a non-classical non-enzyme inhibitor, which can be used for the development of new drugs, especially the research and development of antibacterial drugs.
Preparation Method:
The preparation of anion acid is usually done by synthetic methods. Specifically, the target product can be obtained by reacting benzoyl chloride with Imidazole-1-carboxylic acid, and then adding ammonia water under alkaline conditions to cause amination reaction.
Safety Information:
There is limited information regarding the safety of the. acid. Due to its limited solubility and use, its toxicity and harmfulness have been less studied and evaluated. Regular laboratory safety procedures should be followed in handling and use, and adequate ventilation should be ensured. If necessary, the compound should be used and handled under the guidance of a professional.
Last Update：2024-04-09 21:54:55
