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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-6-methanol

OCc1ccc2c(c1)[nH]nc2 Request for Quotation
Chemical Name: 1H-Indazole-6-methanol
CAS Number: 916902-55-1
Product Number: AG00GUWI(AGN-PC-07135S)
Synonyms:
MDL No:
Molecular Formula: C8H8N2O
Molecular Weight: 148.1619

Identification/Properties

Computed Properties
Molecular Weight:
148.165g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
148.064g/mol
Monoisotopic Mass:
148.064g/mol
Topological Polar Surface Area:
48.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
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 (1H-Indazol-6-yl)methanol compound is a versatile building block in chemical synthesis, offering a diverse range of applications in organic chemistry. Due to its unique structure and reactivity, it serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. This compound can undergo various transformations, such as oxidation, reduction, and substitution reactions, allowing for the introduction of different functional groups. Additionally, the presence of the indazole moiety in its structure imparts specific properties that can be exploited in the design of bioactive molecules and materials with desired characteristics. The application of (1H-Indazol-6-yl)methanol in chemical synthesis enables the efficient and strategic construction of complex molecules, making it a valuable and indispensable tool for organic chemists and researchers in the field.