Pyrrolo[3,4-c]pyrazole, 1,4,5,6-tetrahydro- - Names and Identifiers
Name | 1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole
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Synonyms | LogP 1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole 1,4,5,6-TETRAHYDROPYRROLO[3,4-C]PYRAZOLE 1,4,5,6-Teterahydropyrazolo[3,4-c]pyrazole pyrrolo[3,4-c]pyrazole, 1,4,5,6-tetrahydro- Pyrrolo[3,4-c]pyrazole, 1,4,5,6-tetrahydro-
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CAS | 769895-06-9
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InChI | InChI=1/C5H7N3/c1-4-2-7-8-5(4)3-6-1/h2,6H,1,3H2,(H,7,8) |
Pyrrolo[3,4-c]pyrazole, 1,4,5,6-tetrahydro- - Physico-chemical Properties
Molecular Formula | C5H7N3
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Molar Mass | 109.13 |
Density | 1.267±0.06 g/cm3(Predicted) |
Boling Point | 303.3±32.0 °C(Predicted) |
Flash Point | 137.224°C |
Vapor Presure | 0.001mmHg at 25°C |
Appearance | Crystalline powder |
pKa | 15.58±0.20(Predicted) |
Storage Condition | Room Temprature |
Refractive Index | 1.606 |
MDL | MFCD08447374 |
Pyrrolo[3,4-c]pyrazole, 1,4,5,6-tetrahydro- - Risk and Safety
Pyrrolo[3,4-c]pyrazole, 1,4,5,6-tetrahydro- - Introduction
1,4, 5,6-tetrahydropropyrrolo [3,4-c]pyrazole is an organic compound with the chemical formula C6H9N3. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
1,4, 5,6-tetrahydrobrrolo [3,4-c]pyrazole is a colorless crystalline solid with a low melting point and boiling point. It is stable at room temperature and insoluble in water, but soluble in organic solvents such as ethanol and dimethylformamide. Its structure contains a tetrahydropyrrole ring and a pyrazole ring, and there are some nitrogen atoms in the molecule, so that the compound has a certain degree of reactivity.
Use:
1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole has certain application potential in the field of medicine. It is widely used in the design and synthesis of new drug molecules, such as anti-tumor drugs, antiviral drugs and antibacterial drugs. Its special structure and reactivity make it an important research object.
Preparation Method:
At present, there are various methods for preparing 1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole. Common synthetic methods include cyclization reaction by aziridine, construction reaction of pyrazole ring, etc. The specific synthetic route can be selected according to experimental requirements and specific reaction conditions.
Safety Information:
The safety evaluation of the 1,4, 5,6-tetrahydrobrrolo [3,4-c]pyrazole has not yet been fully completed. Due to its use in the medical field, studies on its toxicity and safety are ongoing. When using and handling the compound, the basic safe handling of chemicals should be observed, such as wearing personal protective equipment, maintaining good ventilation during operation, etc. The relevant safety data sheets should be carefully read and observed before use.
Last Update:2024-04-09 02:00:48