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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-Imidazol-4-yl)boronic acid

OB(c1nc[nH]c1)O Request for Quotation
Chemical Name: (1H-Imidazol-4-yl)boronic acid
CAS Number: 943138-65-6
Product Number: AG005Z7R(AGN-PC-0WAJLC)
Synonyms:
MDL No:
Molecular Formula: C3H5BN2O2
Molecular Weight: 111.8950

Identification/Properties

Properties
BP:
505.2ºC at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(1H-Imidazol-5-yl)boronic acid is a versatile compound commonly used in chemical synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. It serves as a valuable building block in the creation of various functionalized molecules and pharmaceuticals. Due to its boronic acid functionality, this compound can participate in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient construction of complex organic structures. In addition, (1H-Imidazol-5-yl)boronic acid has been employed in the synthesis of biologically active molecules and materials with potential applications in the fields of drug discovery and materials science. Its ability to selectively interact with certain functional groups makes it a valuable tool for organic chemists seeking to design and synthesize novel compounds with specific properties and functions.