1-trityl-1H-pyrazole
1-Triphenylmethyl-pyrazole
CAS: 95163-43-2
Molecular Formula: C22H18N2
1-trityl-1H-pyrazole - Names and Identifiers
| Name | 1-Triphenylmethyl-pyrazole |
| Synonyms | 1-TRITYLPYRAZOLE 1-TRITYLPYRAZOLE 1-Trityl-1H-pyrazole 1-trityl-1H-pyrazole 1-Triphenylmethyl-pyrazole 1-(Triphenylmethyl)-1H-pyrazole 1H-Pyrazole, 1-(triphenylmethyl)- |
| CAS | 95163-43-2 |
| InChI | InChI=1/C22H18N2/c1-4-11-19(12-5-1)22(24-18-10-17-23-24,20-13-6-2-7-14-20)21-15-8-3-9-16-21/h1-18H |
1-trityl-1H-pyrazole - Physico-chemical Properties
| Molecular Formula | C22H18N2 |
| Molar Mass | 310.39 |
| Density | 1.05 |
| Melting Point | 202-204 °C |
| Boling Point | 479.294°C at 760 mmHg |
| Flash Point | 243.668°C |
| Vapor Presure | 0mmHg at 25°C |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| Refractive Index | 1.606 |
| MDL | MFCD09955490 |
1-trityl-1H-pyrazole - Introduction
1-Triphenylmethyl-pyrazole is an organic compound with the chemical formula C19H14N2. The following is a description of the nature, use, preparation and safety information of 1-Triphenylmethyl-pyrazole:
Properties: 1-Triphenylmethyl-pyrazole is a solid compound with a white to light yellow crystal appearance. It has good stability at room temperature and is insoluble in water. Its melting point is 165-167 degrees Celsius.
Purpose: 1-Triphenylmethyl-pyrazole is often used as an intermediate in organic synthesis in the laboratory. It can be converted into other organic compounds, such as ketones, aldehydes and alcohols, through a series of chemical reactions. Due to its unique chemical structure, 1-Triphenylmethyl-pyrazole has also been used in the synthesis and study of organometallic complexes.
Preparation method: The preparation method of 1-Triphenylmethyl-pyrazole is relatively simple. A common synthetic method is by the reaction of tritylammonium iodide and pyrazole. The specific synthesis method can refer to the relevant organic synthesis literature or patent.
Safety information: When handling 1-Triphenylmethyl-pyrazole, general laboratory safety procedures should be followed. This compound has not been extensively studied, so its specific safety information is unclear. During use and storage, avoid contact with strong oxidants and strong acids, and keep away from fire sources. According to the characteristics of the chemical substance, it is recommended to operate in a well-ventilated place and wear suitable protective equipment. If skin contact or inhalation occurs, immediately wash or breathe fresh air and seek medical help if necessary.
Properties: 1-Triphenylmethyl-pyrazole is a solid compound with a white to light yellow crystal appearance. It has good stability at room temperature and is insoluble in water. Its melting point is 165-167 degrees Celsius.
Purpose: 1-Triphenylmethyl-pyrazole is often used as an intermediate in organic synthesis in the laboratory. It can be converted into other organic compounds, such as ketones, aldehydes and alcohols, through a series of chemical reactions. Due to its unique chemical structure, 1-Triphenylmethyl-pyrazole has also been used in the synthesis and study of organometallic complexes.
Preparation method: The preparation method of 1-Triphenylmethyl-pyrazole is relatively simple. A common synthetic method is by the reaction of tritylammonium iodide and pyrazole. The specific synthesis method can refer to the relevant organic synthesis literature or patent.
Safety information: When handling 1-Triphenylmethyl-pyrazole, general laboratory safety procedures should be followed. This compound has not been extensively studied, so its specific safety information is unclear. During use and storage, avoid contact with strong oxidants and strong acids, and keep away from fire sources. According to the characteristics of the chemical substance, it is recommended to operate in a well-ventilated place and wear suitable protective equipment. If skin contact or inhalation occurs, immediately wash or breathe fresh air and seek medical help if necessary.
Last Update：2024-04-10 22:29:15
