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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-chloro-6-(4-methylimidazol-1-yl)pyridazine

Clc1ccc(nn1)n1cnc(c1)C Request for Quotation
Chemical Name: 3-chloro-6-(4-methylimidazol-1-yl)pyridazine
CAS Number: 941294-26-4
Product Number: AG003J9Q(AGN-PC-02TZE9)
Synonyms:
MDL No:
Molecular Formula: C8H7ClN4
Molecular Weight: 194.6210

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
194.622g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
194.036g/mol
Monoisotopic Mass:
194.036g/mol
Topological Polar Surface Area:
43.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
178
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Chloro-6-(4-methyl-1H-imidazol-1-yl)pyridazine, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.In chemical synthesis, 3-Chloro-6-(4-methyl-1H-imidazol-1-yl)pyridazine can be utilized as a key intermediate in the preparation of novel heterocyclic compounds. Its chloro and imidazole functionalities make it a valuable synthon for introducing diverse functional groups, allowing for the modification and diversification of chemical structures.Furthermore, this compound exhibits promising biological activities, making it a valuable candidate for the development of new drugs and bioactive compounds. Its structural features contribute to its potential as a pharmacophore in medicinal chemistry research, with the ability to target specific biological pathways and interactions.Overall, the application of 3-Chloro-6-(4-methyl-1H-imidazol-1-yl)pyridazine in chemical synthesis offers a wide range of opportunities for designing and synthesizing complex molecules with tailored properties for various industrial and scientific applications.