1036248-62-0

Basic information

• Product Name: 1,4-Di(1H-pyrazol-4-yl)benzene
• Synonyms: H2bpzb;1,4-benzenedi(4'-pyrazolyl);1,4-Di(4'-pyrazolyl)benzene, Min. 97%;1,4-Di(1H-pyrazol-4-yl)benzene;1,4-Di(4'-Pyrazolyl)Benzene
• CAS NO: 1036248-62-0
• Molecular Formula: C₁₂H₁₀N₄
• Molecular Weight: 210.2346
• EINECS: -0
• Mol File: 1036248-62-0.mol

Chemical Properties

• Melting Point: >360 °C (sublm)
• Boiling Point: 578.0±43.0 °C(Predicted)
• Appearance: pale yellow/solid
• Density: 1.289±0.06 g/cm3(Predicted)
• PKA: 13.38±0.50(Predicted)
• CAS DataBase Reference: 1,4-Di(1H-pyrazol-4-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Di(1H-pyrazol-4-yl)benzene(1036248-62-0)
• EPA Substance Registry System: 1,4-Di(1H-pyrazol-4-yl)benzene(1036248-62-0)

Safety Data

• Hazardous Substances Data: 1036248-62-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1,4-Di(1H-pyrazol-4-yl)benzene is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs and therapeutic agents.
Used in Material Sciences:
1,4-Di(1H-pyrazol-4-yl)benzene is used as a building block in the creation of new materials with specific properties. Its incorporation into material structures can lead to advancements in areas such as electronics, optics, and energy storage.
Used in Inorganic and Organometallic Chemistry:
1,4-Di(1H-pyrazol-4-yl)benzene is used as a ligand in inorganic and organometallic chemistry. Its ability to form stable complexes with metal ions makes it a valuable component in the synthesis of catalysts and other coordination compounds.
Safety and Handling:
Due to potential hazards associated with the use of 1,4-Di(1H-pyrazol-4-yl)benzene, safety and handling information should be regarded seriously. Proper precautions and protective measures should be taken to minimize risks during its synthesis, storage, and application.

Upstream product

• 1062114-36-6 C₁₂H₁₀O₄ 
• 7325-46-4 1,4-phenylenediacetic acid 
• 106-37-6 1.4-dibromobenzene 

Downstream Products

• 1391524-16-5 2-nitro-1,4-bis(1-H-pyrazol-4-yl)benzene 
• 1391524-18-7 2-amino-1,4-bis(1-H-pyrazol-4-yl)benzene 
• 1391524-20-1 2-hydroxo-1,4-bis(1-H-pyrazol-4-yl)benzene 
• 1391524-23-4 2,5-di(1-H-pyrazol-4-yl)benzenesulfonic acid 

Relevant articles and documents

Facile preparation of polytopic azoles: Synthesis, characterization, and X-ray powder diffraction studies of 1,4-bis(pyrazol-4-yl) and 1,4-bis(tetrazol-5-yl)benzene

Two polytopic azoles, 1,4-bis(pyrazol-4-yl)benzene and 1,4-bis(tetrazol-5- yl)benzene, were prepared in sizable amounts by high yield syntheses employing, in mild conditions, cheap reactants and, whenever possible, aqueous solutions. The two species were

Preparation method of pyrazole-4-aryl derivative

The invention discloses a preparation method of a pyrazole-4-aryl derivative. The preparation method comprises the following step: mixing an aryl halide derivative, a pyrazole-4-boronic acid pinacol ester derivative, first alkali, a first phase transfer catalyst and a first palladium-based catalyst in a first solvent to carry out reaction so as to prepare the pyrazole-4-aryl derivative. Through the manner, the pyrazole-4-aryl derivative is prepared through the adoption of a one-pot method; the reaction condition is mild and the post-treatment is simple and convenient, so that the method is suitable for multiple aryl halide derivatives, strong in operability and suitable for industrial production; and the obtained pyrazole compound can be widely applied to the field of chemical engineering,medicines, biology and materials.

ADSORBENTS WITH STEPPED ISOTHERMS FOR GAS STORAGE APPLICATIONS

The disclosure provides for adsorbents with stepped isotherms for gas storage applications.

Efficient and chromatography-free methodology for the modular synthesis of oligo-(1H-pyrazol-4-yl)-arenes with controllable size, shape and steric bulk

A novel methodology to synthesise oligo-(1H-pyrazol-4-yl)-arenes with controllable size, shape and steric bulk from 1-trityl-1H-pyrazol-4-ylboronate pinacol esters. This straightforward and efficient procedure can be applied to a variety of brominated aro

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Tetranuclear nickel complexes composed of pairs of dinuclear LNi 2 fragments linked by 4,4′-bipyrazolyl, 1,4-bis(4′- pyrazolyl)benzene, and 4,4′-bipyridazine: Synthesis, structures, and magnetic properties

The ability of the ligands 4,4′-bipyrazolyl (H2bpz), 1,4-bis(4′-pyrazolyl)benzene (H2bpzb), and 4,4′- bipyridazine (bpdz) to link two dioctahedral LNi2 units has been examined. The following complexes were prepared: [Lsup