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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)-

[1-(pyridin-3-ylmethyl)pyrazol-4-yl]boronic acid

OB(c1cnn(c1)Cc1cccnc1)O Request for Quotation
Chemical Name: [1-(pyridin-3-ylmethyl)pyrazol-4-yl]boronic acid
CAS Number: 1141888-95-0
Product Number: AG000AQX(AGN-PC-07XUN3)
Synonyms:
MDL No:
Molecular Formula: C9H10BN3O2
Molecular Weight: 203.0056

Identification/Properties

Properties
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


The (1-(Pyridin-3-ylmethyl)-1H-pyrazol-4-yl)boronic acid serves as a versatile and valuable reagent in chemical synthesis due to its unique properties and functional groups. It is commonly utilized in transition metal-catalyzed cross-coupling reactions, particularly in the formation of carbon-carbon bonds. The boronic acid moiety enables selective and efficient coupling with various electrophiles, such as aryl halides or pseudohalides, leading to the construction of complex organic molecules. This compound has found applications in the synthesis of pharmaceuticals, agrochemicals, and materials science due to its ability to facilitate the creation of intricate molecular structures with high efficiency and selectivity.