15953-45-4

Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
5-Chloro-3-methylpyrazole is used as a key building block for the development of new pharmaceuticals and agrochemicals, contributing to the creation of innovative and effective products in these industries.
Used in Catalytic and Analytical Chemistry:
5-Chloro-3-methylpyrazole is utilized as a coordination complexing agent with various metal ions, playing a significant role in enhancing the efficiency and selectivity of catalytic processes and analytical techniques.
Used in Organic Synthesis:
As a reagent, 5-Chloro-3-methylpyrazole is employed in organic synthesis to facilitate specific chemical reactions, contributing to the formation of desired products with greater precision and yield.
Used as a Stabilizer in Chemical Reactions:
5-Chloro-3-methylpyrazole is used to stabilize certain chemical reactions, preventing unwanted side reactions and promoting the desired reaction pathways, thereby improving the overall efficiency and safety of the process.

InChI:InChI=1/C4H5ClN2/c1-3-2-4(5)7-6-3/h2H,1H3,(H,6,7)

Upstream product

• 108-26-9 3-methyl-2-pyrazoline-5-one 
• 54454-10-3 5-chloro-1,3-dimethyl-pyrazole 
• 881668-68-4 5-chloro-1-(2-chlorobenzenesulfonyl)-3-methylpyrazole 
• 4344-87-0 1,2-dihydro-5-methyl-3H-pyrazol-3-one 

Downstream Products

• 51500-32-4 3-chloro-1,5-dimethyl-1H-pyrazole 
• 54454-10-3 5-chloro-1,3-dimethyl-pyrazole 
• 881668-70-8 5-chloro-1H-pyrazole-3-carboxylic acid 
• 861585-71-9 1-benzyl-5-chloro-3-methyl-1H-pyrazole 
• 861585-73-1 1-benzyl-3-chloro-5-methyl-1H-pyrazole 
• 93233-19-3 4-bromo-3-chloro-5-methyl-1H-pyrazole 

Relevant academic research and scientific papers

PYRROLO(PYRAZOLO)PYRIMIDINE DERIVATIVE AS LRRK2 INHIBITOR

The present invention relates to a pyrrolo(pyrazolo)pyrimidine derivative having efficacy as an LRRK2 inhibitor, a preparation method therefor, and a pharmaceutical composition for preventing or treating degenerative brain diseases, containing the same.

3-Substituted pyrazoles and 4-substituted triazoles as inhibitors of human 15-lipoxygenase-1

Investigation of 1N-substituted pyrazole-3-carboxanilides as 15-lipoxygenase-1 (15-LOX-1) inhibitors demonstrated that the 1N-substituent was not essential for activity or selectivity. Additional halogen substituents on the pyrazole ring, however, increased activity. Further development led to triazole-4-carboxanilides and 2-(3-pyrazolyl) benzoxazoles, which are potent and selective 15-LOX-1 inhibitors.

PYRAZOLES USEFUL IN THE TREATMENT OF INFLAMMATION

There is provided compounds of formula (I), wherein R1, R2, A1, A2, A3 and A4 have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of the activit

PYRAZOLES USEFUL IN THE TREATMENT OF INFLAMMATION

There is provided compounds of formula (I), wherein R1, R2, X1, X2 and n have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of the activity of a lipoxygenase (e.g. 15-lipoxygenase) is desired and/or required, and particularly in the treatment of inflammation.

PYRAZOLES USEFUL IN THE TREATMENT OF INFLAMMATION

There is provided compounds of formula (I), wherein R1, R2, X1, X2 and n have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of the activity of a lipoxygenase (e.g. 15-lipoxygenase) is desired and/or required, and particularly in the treatment of inflammation.

PYRAZOLE COMPOUNDS USEFUL IN THE TREATMENT OF INFLAMMATION

There is provided compounds of formula (I), wherein R1, R2, Ra and Rb have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of the activity of a lipoxygenase (e.g. 15-lipoxygenase) is desired and/or required, and particularly in the treatment of inflammation.