1,3-Bis(methyl)imidazolium-2-carboxylate
1,3-Dimethylimidazolium-2-carboxylate
CAS: 536755-29-0
Molecular Formula: C6H8N2O2
1,3-Bis(methyl)imidazolium-2-carboxylate - Names and Identifiers
| Name | 1,3-Dimethylimidazolium-2-carboxylate |
| Synonyms | ium-2-carboxyL 1,3-Dimethylimidazolium-2-carboxylate N,N'-dimethylimidazolium-2-carboxylate 1,3-Bis(methyl)imidazolium-2-carboxylate |
| CAS | 536755-29-0 |
1,3-Bis(methyl)imidazolium-2-carboxylate - Physico-chemical Properties
| Molecular Formula | C6H8N2O2 |
| Molar Mass | 140.14 |
| Melting Point | 221-225°C |
| Solubility | soluble in Methanol |
| Appearance | powder to crystal |
| Color | White to Light yellow to Light orange |
| Storage Condition | 2-8°C |
1,3-Bis(methyl)imidazolium-2-carboxylate - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 41 - Risk of serious damage to eyes |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/39 - |
| WGK Germany | 3 |
1,3-Bis(methyl)imidazolium-2-carboxylate - Introduction
1, is an organic compound with the chemical formula C5H8N2O2. The following is a description of its nature, use, preparation and safety information:
Nature:
1, is a colorless crystalline solid. It is soluble in water and generally less soluble in organic solvents. This compound is a weakly acidic substance.
Use:
1, has a wide range of applications in the field of organic synthesis. It can be used as a catalyst, ligand and one of the solvents for catalytic reactions, such as catalytic olefin epoxidation, asymmetric synthesis and catalytic nucleophilic substitution reactions.
Preparation Method:
1. The preparation of phosphonium can be carried out by a variety of methods. One common method is to react 1,3-dimethylimidazole with an acid to form the corresponding acid salt. This process can be carried out in a suitable solvent.
Safety Information:
1. There is no detailed report on the specific toxicological and safety data of the compound, but it is generally considered to be a relatively safe compound. However, as a chemical substance, it is necessary to pay attention to appropriate laboratory operations and protective measures, such as wearing gloves and goggles, avoiding skin contact and inhalation. During use and storage, it should be kept away from flammable materials and other incompatible substances. For specific safety information, please refer to the compound's Safety Data Sheet (MSDS) or consult a professional.
Nature:
1, is a colorless crystalline solid. It is soluble in water and generally less soluble in organic solvents. This compound is a weakly acidic substance.
Use:
1, has a wide range of applications in the field of organic synthesis. It can be used as a catalyst, ligand and one of the solvents for catalytic reactions, such as catalytic olefin epoxidation, asymmetric synthesis and catalytic nucleophilic substitution reactions.
Preparation Method:
1. The preparation of phosphonium can be carried out by a variety of methods. One common method is to react 1,3-dimethylimidazole with an acid to form the corresponding acid salt. This process can be carried out in a suitable solvent.
Safety Information:
1. There is no detailed report on the specific toxicological and safety data of the compound, but it is generally considered to be a relatively safe compound. However, as a chemical substance, it is necessary to pay attention to appropriate laboratory operations and protective measures, such as wearing gloves and goggles, avoiding skin contact and inhalation. During use and storage, it should be kept away from flammable materials and other incompatible substances. For specific safety information, please refer to the compound's Safety Data Sheet (MSDS) or consult a professional.
Last Update：2024-04-10 22:29:15
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