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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)-

Ethanone, 1-(6-chloroimidazo[1,2-b]pyridazin-3-yl)-

Clc1ccc2n(n1)c(cn2)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-(6-chloroimidazo[1,2-b]pyridazin-3-yl)-
CAS Number: 90734-71-7
Product Number: AG003D1T(AGN-PC-00LOSR)
Synonyms:
MDL No: MFCD11044766
Molecular Formula: C8H6ClN3O
Molecular Weight: 195.6057

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
195.606g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
195.02g/mol
Monoisotopic Mass:
195.02g/mol
Topological Polar Surface Area:
47.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
223
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone is a versatile intermediate used in chemical synthesis for the preparation of various functionalized derivatives. Its unique structure containing a substituted imidazo[1,2-b]pyridazine moiety offers a platform for introducing diverse chemical functionalities through synthetic transformations. In organic synthesis, this compound can serve as a building block for the construction of heterocyclic compounds with potential pharmaceutical or material science applications. Its reactivity allows for the incorporation of different substituents or functional groups, enabling the creation of novel compounds with tailored properties. Additionally, the presence of the chloro substituent provides a handle for further derivatization, facilitating the synthesis of more complex molecules. The use of 1-(6-Chloroimidazo[1,2-b]pyridazin-3-yl)ethanone in chemical synthesis highlights its importance as a key intermediate for accessing structurally diverse compounds with potential biological or material applications.