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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)-

5-Acetyl-1-methyl-1H-indazole.

CC(=O)c1ccc2c(c1)cnn2C Request for Quotation
Chemical Name: 5-Acetyl-1-methyl-1H-indazole.
CAS Number: 1159511-24-6
Product Number: AG000H6K(AGN-PC-0WAJXZ)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O
Molecular Weight: 174.1992

Identification/Properties

Computed Properties
Molecular Weight:
174.203g/mol
XLogP3:
1.3
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:
34.9A^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


1-(1-Methyl-1H-indazol-5-yl)ethanone, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis processes. Its unique molecular structure makes it a valuable intermediate in the production of various organic compounds.One of the key applications of $name$ in chemical synthesis is as a building block for the synthesis of pharmaceuticals and fine chemicals. Its presence in the molecular structure of these compounds imparts specific properties and functionalities essential for their biological activity and interactions. By incorporating $name$ into target molecules, chemists can effectively introduce the indazole moiety, thus modulating the pharmacological profile of the final product.Moreover, the reactivity of the ethanone functional group in $name$ allows for further derivatization through various chemical reactions. This enables chemists to introduce additional functional groups or modify the structure to tailor the properties of the final compound for specific applications. Additionally, the indazole ring system in $name$ can participate in diverse synthetic transformations, expanding the scope of its utility in the synthesis of complex organic molecules.In summary, the strategic incorporation of 1-(1-Methyl-1H-indazol-5-yl)ethanone in chemical synthesis processes facilitates the efficient construction of diverse organic compounds, particularly in the pharmaceutical and fine chemical industries. Its role as a versatile building block underscores its significance in enabling the synthesis of novel molecules with tailored properties and enhanced functionalities.