10344-42-0

Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-3,6-dichloropyridazine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable component in the development of new drugs and medicinal agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Bromo-3,6-dichloropyridazine is employed as a precursor in the production of pesticides and other crop protection agents. Its properties contribute to the effectiveness of these products in managing pests and diseases in agriculture.
Used in Material Science:
4-Bromo-3,6-dichloropyridazine is utilized as a building block in the synthesis of advanced materials with specific properties for use in various applications within material science. Its versatility allows for the creation of materials with tailored characteristics to meet industry demands.
Used in Chemical Synthesis:
As a key intermediate in chemical synthesis, 4-Bromo-3,6-dichloropyridazine is used for the preparation of a wide range of chemical compounds. Its reactivity and structural features make it an essential component in the development of new chemical entities for diverse applications.

InChI:InChI=1/C4HBrCl2N2/c5-2-1-3(6)8-9-4(2)7/h1H

Upstream product

• 15456-86-7 4-bromo-1,2-dihydropyridazine-3,6-dione 

Downstream Products

• 21415-33-8 3,6-dichloro-4-pyrrolidin-1-yl-pyridazine 
• 10344-41-9 2-[(3,6-dichloropyridazine-4-yl)thio]aniline 
• 823-58-5 3,6-dichloropyridazin-4-amine 

Relevant academic research and scientific papers

Synthesis of new derivatives of 10H-benzo[b]pyridazino[3,4-e][1,4]thiazines

New 10H-benzo[b]pyridazino[3,4-e][1,4]thiazines were prepared and evaluated for inhibitory activity against soybean 15-lipoxygenase enzyme. These compounds were synthesized by the sequential treatment of 4-bromo-3,6-dichloropyridazine with 2-aminothiophenol and a secondary amine with the subsequent heterocyclization in the presence of sodium amide.

DERIVATIVES AND ANALOGS OF N-ETHYLQUINOLONES AND N-ETHYLAZAQUINOLONES

Bicyclic nitrogen containing compounds and their use as antibacterials.

PYRROLO-QUINOXALINONE DERIVATIVES AS ANTIBACTERIALS

Tricyclic nitrogen containing compounds of the following Formula (I) and their use as antibacterials.

Triazolo-pyridazine derivatives as ligands for GABA receptors

1,2,4-triazolo[4,3-b]pyridazine derivatives, possessing an optionally substituted cycloalkyl, phenyl or heteroaryl substituent at the 3-position, a substituted alkoxy moiety at the 6-position, an optionally substituted N-linked nitrogen-containing aliphat

Triazolo-pyridazine derivatives as ligands for GABA receptors

1,2,4-triazolo[4,3-b]pyridazine derivatives, possessing a fluoro-substituted phenyl ring at the 3-position and a heteroaryl-alkoxy moiety at the 6-position, are selective ligands for GABAAreceptors, in particular having high affinity for the α2

Triazolo-pyridazine derivatives as ligands for GABA receptors

1,2,4-triazolo[4,3-b]pyridazine derivatives, represented by wherein Z represents cyclobutyl or pyrrolidin-1-yl, are selective ligands for GABAAreceptors, in particular having high affinity for the α2 and/or α3 subunit thereof, are useful in the

Substituted triazolo-pyridazine derivatives as ligands for GABA receptors

Substituted triazolo-pyridazine derivative compounds represented by wherein the variables are disclosed herein are selective ligands for GABA-A receptors, particularly for the α2 and/or α3 subunits.

Triazolo-pyridazine derivatives as ligands for GABA receptors

1,2,4-triazolo[4,3-b]pyridazine derivatives, represented by wherein Z represents cyclobutyl, 1-methylcyclopentyl or pyrrolidin-1-yl, are selective ligands for GABAAreceptors, in particular having high affinity for the α2 and/or α3 subunit there

Triazolo-pyridazine derivatives as ligands for GABA receptors

1,2,4-triazolo[4,3-b]pyridazine derivatives, represented by wherein Z represents an optionally substituted tetrahydropyridinyl substituent, are selective ligands for GABAAreceptors, in particular having high affinity for the α2 and/or α3 subuni