7231-31-4

Usage

Uses

Used in Medicinal Chemistry:
3-Propyl-1H-pyrazole is used as a building block for the synthesis of pharmaceuticals and agrochemicals due to its molecular structure and properties. It contributes to the development of new compounds with potential biological activities and pharmacological properties.
Used in Material Science:
3-Propyl-1H-pyrazole is used in the development of new materials and chemical processes due to its structural features. Its unique properties may enable the creation of innovative materials with specific characteristics for various applications.

InChI:InChI=1/C6H10N2/c1-2-3-6-4-5-7-8-6/h4-5H,2-3H2,1H3,(H,7,8)

Upstream product

• 58953-13-2 (1E)-1-chlorohex-1-en-3-one 
• 107-87-9 2-Pentanone 
• 109-94-4 formic acid ethyl ester 
• 64-17-5 ethanol 
• 7803-57-8 hydrazine hydrate 
• 106-94-5 propyl bromide 
• 107073-66-5 α,γ-dipyrrolidinylglutaronitrile 

Relevant academic research and scientific papers

Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with azaindoleoxoacetyl piperazine derivatives. These compounds possess unique antiviral activity, whether used alone or in combination with other antivirals, antiinfectives, immunomodulators or HIV entry inhibitors. More particularly, the present invention relates to the treatment of HIV and AIDS.

Indole, azaindole and related heterocyclic 4-alkenyl piperidine amides

This invention provides compounds having drug and bio-affecting properties, their pharmaceutical compositions and method of use. In particular, the invention is concerned with new piperidine 4-alkenyl derivatives that possess unique antiviral activity. More particularly, the present invention relates to compounds useful for the treatment of HIV and AIDS. The compounds of the invention for the general Formula I: wherein: Z is Q is selected from the group consisting of: —W— is

A NEW SYNTHESIS OF 3,5-DISUBSTITUTED PYRAZOLES BY REACTION OF α,γ-DIPYROLIDINYLGLUTARONITRILES (MASKED α,γ-DIKETONE EQUIVALENTS) WITH HYDRAZINES

An efficient sequence proposed for a new synthetic method of 3,5-disubstituted pyrazoles involves the reaction of α,γ-dipyrolidinylglutaronitriles (masked α,γ-diketone equivalents) with hydrazines.