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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-(1-methyl-1H-indazol-3-yl)-

CC(=O)c1nn(c2c1cccc2)C Request for Quotation
Chemical Name: Ethanone, 1-(1-methyl-1H-indazol-3-yl)-
CAS Number: 69271-42-7
Product Number: AG006NF2(AGN-PC-0NJ0XU)
Synonyms:
MDL No:
Molecular Formula: C10H10N2O
Molecular Weight: 174.1992

Identification/Properties

Properties
MP:
88-90℃(Solv: hexane (110-54-3))
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
174.203g/mol
XLogP3:
1.6
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


The compound 1-(1-Methyl-1H-indazol-3-yl)ethanone is a versatile building block in chemical synthesis. Its unique structure allows for a variety of reactions and transformations, making it a valuable tool for organic chemists.In chemical synthesis, 1-(1-Methyl-1H-indazol-3-yl)ethanone can be utilized as a key intermediate in the production of various pharmaceuticals, agrochemicals, and other fine chemicals. Its functional groups enable it to participate in a range of reactions, such as nucleophilic addition, substitution, and condensation reactions.Furthermore, the presence of the indazole moiety in 1-(1-Methyl-1H-indazol-3-yl)ethanone makes it particularly useful in the synthesis of heterocyclic compounds, which are prevalent in many biologically active molecules. This compound serves as a valuable starting material for the construction of complex organic structures with diverse pharmacological and industrial applications.