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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)-

Imidazo[1,2-b]pyridazine-2-carboxylic acid, 6-chloro-

Clc1ccc2n(n1)cc(n2)C(=O)O Request for Quotation
Chemical Name: Imidazo[1,2-b]pyridazine-2-carboxylic acid, 6-chloro-
CAS Number: 14714-24-0
Product Number: AG001ENP(AGN-PC-0KL6ZZ)
Synonyms:
MDL No:
Molecular Formula: C7H4ClN3O2
Molecular Weight: 197.5786

Identification/Properties

Computed Properties
Molecular Weight:
197.578g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
196.999g/mol
Monoisotopic Mass:
196.999g/mol
Topological Polar Surface Area:
67.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
226
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloroimidazo[1,2-b]pyridazine-2-carboxylic acid is a versatile compound that finds extensive application in chemical synthesis. Due to its unique structure and reactivity, this compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. In organic synthesis, 6-Chloroimidazo[1,2-b]pyridazine-2-carboxylic acid can be utilized as a key intermediate for the preparation of complex heterocyclic compounds. Its functional groups enable it to participate in a range of coupling reactions, including Suzuki and Buchwald-Hartwig cross-coupling reactions, allowing for the introduction of diverse substituents. Moreover, this compound can be employed in ring-closing reactions to form fused heterocycles with enhanced biological activities. Its significance as a versatile synthetic precursor makes it an indispensable tool for chemists seeking to access structurally diverse molecules with potential applications in drug discovery and material science.