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Usage

Uses

Used in Epoxy Resin Industry:
1-ALLYL-3,5-DIMETHYLPYRAZOLE 96 is used as a curing agent for epoxy resins, providing enhanced thermal stability and performance in applications that demand heat resistance.
Used in Pharmaceutical Production:
In the pharmaceutical sector, 1-ALLYL-3,5-DIMETHYLPYRAZOLE 96 serves as an intermediate in the synthesis of various drugs, contributing to the development of new medicinal compounds.
Used in Agrochemical Industry:
Similarly, in agrochemicals, 1-ALLYL-3 5-DIMETHYLPYRAZOLE 96 acts as an intermediate, playing a crucial role in the production of crop protection agents and other agricultural products.
Used in Polymer Stabilization:
1-ALLYL-3,5-DIMETHYLPYRAZOLE 96 is utilized as a stabilizer in the manufacturing of polymers to improve their resistance to thermal degradation, thereby extending their service life and performance.
Used in Adhesive and Sealant Manufacturing:
As an additive in the production of adhesives and sealants, 1-ALLYL-3 5-DIMETHYLPYRAZOLE 96 enhances the bonding properties and durability of these materials, making them suitable for a wide range of applications.

InChI:InChI=1/C8H12N2/c1-4-5-10-8(3)6-7(2)9-10/h4,6H,1,5H2,2-3H3

Upstream product

• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 106-95-6 allyl bromide 
• 694-48-4 1,3-dimethyl-1H-pyrazole 
• 123-54-6 acetylacetone 
• 41736-95-2 spiro[adamantane-2,3'-diazirine] 
• 1730-25-2 allylmagnesium bromide 

Downstream Products

• 1155595-91-7 1-allyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde 
• 13369-76-1 1-allyl-4-bromo-3,5-dimethyl-1H-pyrazole 
• 1563062-64-5 ethyl ({4-[(4-chlorophenyl)sulfanyl]-1-(3,5-dimethyl-1H-pyrazol-1-yl)-4,4-difluorobutan-2-yl}sulfanyl)methanethioate 
• 67-51-6 3,5-dimethyl-1H-pyrazole 

Relevant academic research and scientific papers

2-(pyrazol-4-yl)-1,3-oxaselenolanes from pyrazole carbaldehydes and 2-selanyl-1-ethanol

Pyrazole carbaldehydes react with 2-selanyl-1-ethanol at room temperature in the presence of trimethylchlorosilane followed by treatment C with triethyl amine to afford the corresponding 2-(pyrazol-4-yl)-1,3-oxaselenolanes. The structure of the novel compounds was confirmed by IR, 13 C, 1 H, 15N, and 77 Se NMR spectroscopy.this article online at wileyonlinelibrary.com.

Synthesis of heterocyclic compounds from 4-formylpyrazoles

Formylation of pyrazole and 2,5-dimethylpyrazole gave a number of pyrazole-containing aldehydes, which can be used to obtain chromenes, tetrahydrochromenes, 1,4-dihydropyrano[2,3-c]pyrazoles, pyrano[3,2-c]chromenes, thiochromeno[4,3-b]pyrans, pyrano[3,2-c

Diazirines as potent electrophilic Nitrogen sources: Application to the synthesis of Pyrazoles

Even after more than 50 years since its discovery, the electrophilic potential of diazirines was never truly exploited. This longstanding limitation has been resolved. N-Monosubstituted diaziridines and hydrazones are obtained by nucleophilic additions. They release, under hydrolysis conditions, the corresponding monosubstituted hydrazines. The latter were converted to pyrazoles in high yields. The adamantanone can be recovered in 80-100% yields. This work demonstrates the potential of diazirines as electrophilic nitrogen sources with recoverable protecting groups.