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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-(2-methylimidazo[1,2-a]pyridin-3-yl)-

CC(=O)c1c(C)nc2n1cccc2 Request for Quotation
Chemical Name: Ethanone, 1-(2-methylimidazo[1,2-a]pyridin-3-yl)-
CAS Number: 29096-60-4
Product Number: AG002XAI(AGN-PC-0KK6Z2)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O
Molecular Weight: 174.1992

Identification/Properties

Computed Properties
Molecular Weight:
174.203g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
174.079g/mol
Monoisotopic Mass:
174.079g/mol
Topological Polar Surface Area:
34.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
217
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


The compound 1-(2-Methylimidazo[1,2-a]pyridin-3-yl)ethanone, also known as $name$, is a valuable chemical reagent in organic synthesis. With its unique structure, this compound serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. It can undergo various functional group transformations, making it a crucial intermediate in the synthesis of complex molecules. Additionally, the presence of the imidazole and pyridine rings in its structure imparts specific properties that are beneficial for designing new chemical entities with desired biological or physical characteristics. Through strategic use in chemical reactions, $name$ enables chemists to access diverse molecular architectures efficiently, facilitating the development of novel compounds with potential applications in drug discovery and materials science.