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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-4-boronic acid

OB(c1cccc2c1cn[nH]2)O Request for Quotation
Chemical Name: 1H-Indazole-4-boronic acid
CAS Number: 1023595-17-6
Product Number: AG00078T(AGN-PC-0712JE)
Synonyms:
MDL No:
Molecular Formula: C7H7BN2O2
Molecular Weight: 161.9537

Identification/Properties

Computed Properties
Molecular Weight:
161.955g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
162.06g/mol
Monoisotopic Mass:
162.06g/mol
Topological Polar Surface Area:
69.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
168
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Indazole-4-boronic acid is a versatile compound widely used in organic synthesis due to its unique properties and reactivity. As a boronic acid derivative, it serves as a key building block in the preparation of various functionalized indazole derivatives. Its ability to participate in Suzuki-Miyaura cross-coupling reactions makes it an essential tool in the construction of carbon-carbon bonds, enabling the efficient synthesis of biologically active molecules, pharmaceuticals, and materials. Additionally, 1H-Indazole-4-boronic acid can be employed as a valuable ligand in transition metal-catalyzed reactions, leading to the formation of complex molecular structures with diverse applications in medicinal chemistry and material science. Its broad utility and compatibility with a range of synthetic methodologies highlight its significant role in advancing chemical research and development.