7554-67-8

Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrazole, 4-ethyl-3,5-dimethylis used as a building block for the development of various drugs, contributing to the creation of new pharmaceutical compounds with potential therapeutic benefits.
Used in Agrochemical Industry:
Ethylmethylpyrazole is used in the field of agrochemicals, potentially serving as a component in the development of new agrochemical products for agricultural applications.
Used in Organic Synthesis:
1H-Pyrazole, 4-ethyl-3,5-dimethylis used as a reagent in organic synthesis, aiding in the production of a range of organic compounds for various purposes.
Used in Materials Science:
Ethylmethylpyrazole may have potential uses in the field of materials science, possibly contributing to the development of new materials with unique properties.
Used as a Catalyst in Chemical Reactions:
1H-Pyrazole, 4-ethyl-3,5-dimethylmay also be utilized as a catalyst in chemical reactions, facilitating specific processes and potentially improving the efficiency of certain chemical syntheses.

Upstream product

• 1540-34-7 3-ethyl-2,4-pentanedione 
• 75326-05-5 3-Ethyl-3,5-dimethyl-3H-pyrazole 
• 75-03-6 ethyl iodide 
• 21981-22-6 3,5-Dimethyl-5-ethyl-Δ²-pyrazolin 

Relevant academic research and scientific papers

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.

FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS

A series of 6,7-dihydro[1,3]thiazolo[5,4-c]pyridin-4(5H)-one derivatives, and analogues thereof, which are substituted in the 2-position by an optionally substituted morpholin-4-yl moiety, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, oncological, nociceptive or ophthalmic conditions.

MIGRATION TENDENCIES OF FUNCTIONAL GROUPS TOWARD SIGMATROPIC REARRANGEMENT IN 3,3-DISUBSTITUTED 3H-PYRAZOLES

3,3-Disubstituted 3H-pyrazoles la - e aromatise through an intramolecular sigmatropic 1,5-(1,2-)shift of one of the quaternary groups.From a kinetic study of the uncatalysed and of the acid catalysed isomerisation reaction migration tendencies of functional groups in sigmatropic rearrangement toward neutral and toward cationic centers are obtained.