3,5-DI(2-PYRIDYL)PYRAZOLE - Names and Identifiers
Name | 3,5-DI(2-PYRIDYL)PYRAZOLE
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Synonyms | Dipyridylpyrazole 3,5-DI(2-PYRIDYL)PYRAZOLE 2,2-(1H-Pyrazole-3,5-diyl)dipyridine 2,2'-(1H-Pyrazole-3,5-diyl)dipyridine Pyridine, 2,2-(1H-pyrazole-3,5-diyl)bis- Pyridine, 2,2'-(1H-pyrazole-3,5-diyl)bis- 2-[5-(2-Pyridinyl)-1H-pyrazol-3-yl]pyridine
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CAS | 129485-83-2
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3,5-DI(2-PYRIDYL)PYRAZOLE - Physico-chemical Properties
Molecular Formula | C13H10N4
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Molar Mass | 222.25 |
Density | 1.248±0.06 g/cm3(Predicted) |
Melting Point | 188 °C |
Boling Point | 476.5±35.0 °C(Predicted) |
pKa | 9.96±0.19(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2-8°C |
MDL | MFCD00130125 |
3,5-DI(2-PYRIDYL)PYRAZOLE - Risk and Safety
Hazard Symbols | Xn - Harmful
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Risk Codes | 22 - Harmful if swallowed
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3,5-DI(2-PYRIDYL)PYRAZOLE - Upstream Downstream Industry
3,5-DI(2-PYRIDYL)PYRAZOLE - Introduction
3,5-di (2-PYRIDYL)PYRAZOLE is an organic compound with the chemical formula C10H8N4. It has some of the following properties:
1. Appearance: 3,5-di (2-PYRIDYL)PYRAZOLE is a white to pale yellow solid.
2. Solubility: It has good solubility in common organic solvents.
3. Melting point and boiling point: its melting point is 132-135 degrees Celsius.
4. Stability: 3,5-di (2-pyriridyl) PYRAZOLE is a relatively stable compound, which can exist stably under regular environmental conditions.
3,5-di (2-PYRIDYL)PYRAZOLE has many uses, including but not limited to the following:
1. Coordination chemistry: Because it contains two coordination sites, it can be used as a ligand to form complexes with transition metal ions, which is used in the fields of catalyst, photochemistry and bio-inorganic chemistry.
2. Analytical chemistry: It can be used as an analytical reagent for the detection and quantitative analysis of metal ions.
3. Organic synthesis: 3,5-di (2-PYRIDYL)PYRAZOLE is a versatile organic synthesis intermediate that can be used to prepare other organic compounds.
There are many methods for preparing 3,5-di (2-PYRIDYL)PYRAZOLE, one of which is commonly used as follows:
1. First, pyridine was dissolved in sodium hydroxide solution.
2. Under stirring, Chloroacetyl Chloride is slowly added dropwise to react to generate 2-pyridyl pyrazole.
3. Reaction of 2-pyridylpyrazole with excess pyridine bromide to generate 3,5-di (2-pyriridyl) PYRAZOLE.
4. The pure product is obtained by appropriate process steps such as crystallization, filtration and drying.
Regarding safety information, 3,5-di (2-PYRIDYL)PYRAZOLE has no clear risk report at this time. However, as a chemical, some safety measures still need to be taken:
1. Avoid contact with skin, eyes and respiratory system.
2. Use appropriate protective equipment such as laboratory gloves, safety glasses and protective masks when handling and handling.
3. Keep away from ignition and flammable materials during use and storage.
4. Follow laboratory rules and regulations, dispose of waste properly, and comply with local and national regulations. In case of uncertainty, professional bodies or experienced personnel should be consulted.
Last Update:2024-04-10 22:43:14