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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-indazol-5-ylboronic acid

OB(c1ccc2c(c1)cn[nH]2)O Request for Quotation
Chemical Name: 1H-indazol-5-ylboronic acid
CAS Number: 338454-14-1
Product Number: AG0038TM(AGN-PC-01LR8A)
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Indazole-5-boronic acid is a versatile chemical compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, it serves as a valuable building block for the construction of various organic molecules and pharmaceutical compounds. This boronic acid derivative is particularly important in the field of medicinal chemistry, where it is employed in the preparation of potential drug candidates and bioactive molecules. Its boronic acid functionality enables selective Suzuki-Miyaura cross-coupling reactions, allowing for the efficient formation of carbon-carbon bonds under mild conditions. Additionally, 1H-Indazole-5-boronic acid plays a crucial role in the development of agrochemicals, materials science, and other areas of organic synthesis, making it a key component in modern chemical research and development.