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Usage

Uses

Used in Pharmaceutical Industry:
1-Propyl-1H-pyrazole is used as an intermediate in the synthesis of various organic compounds for the development of new drugs and pharmaceutical products. Its unique structure and properties make it a valuable building block in medicinal chemistry.
Used in Agrochemical Industry:
1-Propyl-1H-pyrazole is used as a component in the formulation of agrochemicals, such as pesticides and herbicides. Its potential biological activities contribute to the effectiveness of these products in controlling pests and weeds in agricultural settings.
Used in Materials Science:
1-Propyl-1H-pyrazole is used as a building block in the development of new materials with specific properties. Its versatile chemical structure allows for the creation of materials with tailored characteristics for various applications in materials science.
Used in Research and Development:
1-Propyl-1H-pyrazole is used as a research compound for studying its potential biological activities and exploring its role as a ligand for targeting specific receptors and enzymes in the body. This research can lead to the discovery of new therapeutic agents and a better understanding of biological processes.
Overall, 1-Propyl-1H-pyrazole is a significant chemical compound with diverse applications in various fields, making it an essential component in the development of new products and advancements in science and technology.

InChI:InChI=1/C6H10N2/c1-2-5-8-6-3-4-7-8/h3-4,6H,2,5H2,1H3

Upstream product

• 288-13-1 NH-pyrazole 
• 106-94-5 propyl bromide 
• 627-18-9 1-bromo-3-propanol 

Downstream Products

• 141302-33-2 4-bromo-1-propyl-1H-pyrazole 
• 1006458-89-4 C₇H₁₀N₂O 
• 847818-76-2 1-propyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 

Relevant academic research and scientific papers

Protonated alkylpyrazole ionic liquid and method using same for synthesizing cyclic carbonate

The invention relates to protonated alkylpyrazole ionic liquid with a structural formula as shown in the description, wherein n is equal to 1, 2, 3 or 4, and X is Cl, Br or I. The invention further discloses a method for synthesizing cyclic carbonate by using the protonated alkylpyrazole ionic liquid; the protonated alkylpyrazole ionic liquid and an epoxy compound are added into a high-pressure reaction kettle according to a molar ratio of 1 : (25 to 300), CO2 is introduced until pressure is 1-3 MPa, and constant-temperature constant-pressure reaction is performed for 1-5 hours at a temperature of 100-150 DEG C, and post-treatment is performed after reaction is ended, thus obtaining the cyclic carbonate. The method solves the problems that CO2 activation is difficulty, a catalyst is dear, a poisonous organic solvent is used, a synthesis process is complex, reaction conditions are harsh and the like in an existing method. The advantages of simple synthesis process, high catalyst activity, environmental friendliness, low cost and the like are achieved.

NEW THIENOPYRIMIDINE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

Compounds of formula (I): wherein R1, R2, R3, R4, R5, R6, R7, R12, X, A and n are as defined in the description.

Synthesis of pinacol esters of 1-alkyl-1H-pyrazol-5-yl- and 1-alkyl-1H-pyrazol-4-ylboronic acids

Starting from 1H-pyrazol, a wide number of 1-alkyl-1H-pyrazol-4-yl and 1-alkyl-1H-pyrazol-5-ylboronic acids and their pinacol esters were synthesized and characterized. The key step in the described methodology is the regioselective lithiation of the pyrazole ring. The synthesized pinacolates are stable under prolonged storage and can be used as convenient reagents in organic synthesis.