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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)-

1H-Indazole, 5-methyl-

Cc1ccc2c(c1)cn[nH]2 Request for Quotation
Chemical Name: 1H-Indazole, 5-methyl-
CAS Number: 1776-37-0
Product Number: AG0025F0(AGN-PC-0NJPPY)
Synonyms:
MDL No:
Molecular Formula: C8H8N2
Molecular Weight: 132.1625

Identification/Properties

Computed Properties
Molecular Weight:
132.166g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
132.069g/mol
Monoisotopic Mass:
132.069g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
124
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


5-Methyl-1H-indazole is a versatile compound frequently utilized in chemical synthesis due to its unique chemical properties and reactivity. As a heterocyclic aromatic molecule, 5-Methyl-1H-indazole serves as a valuable building block in the creation of various organic compounds. In synthetic chemistry, this indazole derivative is employed in the development of pharmaceuticals, agrochemicals, and materials science applications. Its structural features make it a crucial intermediate in the synthesis of specialized reagents and complex organic molecules. Additionally, 5-Methyl-1H-indazole demonstrates promising potential in the construction of novel heterocyclic frameworks with diverse functional groups, showcasing its significance as a valuable tool for modern chemical synthesis methodologies.