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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)-

[5-methyl-6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridin-3-yl]boronic acid

O=C(OC(C)(C)C)Nc1ncc(cc1C)B(O)O Request for Quotation
Chemical Name: [5-methyl-6-[(2-methylpropan-2-yl)oxycarbonylamino]pyridin-3-yl]boronic acid
CAS Number: 1356087-58-5
Product Number: AG009XTR(AGN-PC-0JF3XP)
Synonyms:
MDL No:
Molecular Formula: C11H17BN2O4
Molecular Weight: 252.07468

Identification/Properties

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 (6-((tert-Butoxycarbonyl)amino)-5-methylpyridin-3-yl)boronic acid is a versatile compound widely utilized in chemical synthesis. It serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials. This compound is particularly valued for its ability to act as a ligand in transition-metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Chan-Lam couplings. Additionally, its boronic acid functionality allows for efficient C-C bond formation, making it an essential tool in the construction of complex organic molecules. Moreover, the tert-butoxycarbonyl (Boc) protecting group enhances the compound's stability and enables selective manipulation of its reactivity, further expanding its applicability in organic synthesis strategies.