4345-49-7

Basic information

• Product Name: 1H-Pyrazole, 3,5-dimethyl-4-phenyl-
• Synonyms: 3,5-Dimethyl-4-phenyl-1H-pyrazol;3,5-Dimethyl-4-phenylpyrazol;3,5-Dimethyl-4-phenyl-pyrazol;3,5-dimethyl-4-phenylpyrazole;2,4-dimethyl-3-phenyl-pyrazole;3,5-Dimethyl-4-phenyl-1H-pyrazole
• CAS NO: 4345-49-7
• Molecular Formula: C11H12N2
• Molecular Weight: 172.23
• Mol File: 4345-49-7.mol
• Article Data: 7

Chemical Properties

• Melting Point: 170 - 171 °C
• CAS DataBase Reference: 1H-Pyrazole, 3,5-dimethyl-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrazole, 3,5-dimethyl-4-phenyl-(4345-49-7)
• EPA Substance Registry System: 1H-Pyrazole, 3,5-dimethyl-4-phenyl-(4345-49-7)

Safety Data

• Hazardous Substances Data: 4345-49-7(Hazardous Substances Data)

Usage

Chemical structure

1H-Pyrazole ring with two methyl groups (CH3) and a phenyl group (C6H5) attached.

Versatile reactivity

Can react with a variety of other chemicals, making it useful in the synthesis of pharmaceuticals and agrochemicals.

Biological activity

Has been studied for its potential anti-inflammatory, antifungal, and anticancer properties.

Building block for drug discovery

Valuable component in the development of new drugs due to its potential therapeutic properties.

Use in material development

Has potential for use in the development of novel materials.

Precursor in organic synthesis

Can be used as a starting material for the synthesis of other organic compounds.

Upstream product

• 103858-98-6 2-(3,5-dimethyl-1⁽²⁾H-pyrazol-4-yl)-aniline 
• 705-60-2 1-phenyl-2-nitroprop-1-ene 
• 79-24-3 Nitroethane 
• 108-86-1 bromobenzene 
• 857530-80-4 3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 
• 3398-16-1 4-Bromo-3,5-dimethylpyrazole 
• 98-80-6 phenylboronic acid 
• 75326-06-6 3,5-Dimethyl-3-phenyl-3H-pyrazole 
• 5910-25-8 3-phenylpentane-2,4-dione 

Downstream Products

• 59843-47-9 2-(3,5-dimethyl-4-phenyl-pyrazol-1-yl)-N,N-dimethyl-propionamide 
• 616879-81-3 ethyl 6-(3,5-dimethyl-4-phenyl-1H-pyrazol-1-yl)nicotinate 

Relevant articles and documents

Tetravalent metal platinum complex containing tetradentate ligand, preparation method, application and device

The invention relates to the technical field of organic luminescent materials and provides a tetravalent metal platinum complex phosphorescent luminescent material containing a tetradentate ligand. The tetravalent metal platinum complex containing the tetradentate ligand has a structure shown in a first general formula. Meanwhile, the invention also provides a preparation method of the tetravalentmetal platinum complex containing the tetradentate ligand, an application of the tetravalent metal platinum complex containing the tetradentate ligand in an electroluminescent device and a device, the device comprises the tetravalent metal platinum complex containing the tetradentate ligand. According to the tetravalent metal platinum complex containing the tetradentate ligand, the structure of the ligand surrounding the metal center and the structure of the substituent group on the ligand are regulated and controlled to regulate and control the photophysical property of the tetradentate ringmetal platinum complex, and the tetravalent metal platinum complex has the advantage of high stability and has wide application prospect in a plurality of fields such as OLED display, illumination and the like.

Tetradentate cyclometalated platinum complex containing 6-substituted carbazole and preparation method and application thereof

The invention relates to the field of blue phosphorescent tetradentate cyclometalated platinum complexes and discloses a blue phosphorescent tetradentate cyclometalated platinum complex with 6-substituted carbazole and a preparation method and application thereof. The complex herein may be a delayed fluorescent and/or phosphorescent emitter, having the advantages of high thermo-decomposition temperature, great quantum effect, blue emission, narrow emission spectrum and the like; therefore, the complex has a great application prospect in the field of blue light material, particularly the fieldof deep blue phosphorescent materials.

Nitrogen-containing heterocycles from metal β-diketonates

Factors determining the reaction of metal β-diketonates with hydrazine, in particular the nature of central metal ion and structure of β-diketonate ligand, are discussed. The possibility for the preparation of other heterocyclic compounds via reaction of metal acetylacetonates with phenylhydrazine, o-phenylenediamine, urea, and thiourea was studied.