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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)-

2-(tert-ButoxycarbonylaMino)pyridin-4-ylboronic acid

OB(c1ccnc(c1)NC(=O)OC(C)(C)C)O Request for Quotation
Chemical Name: 2-(tert-ButoxycarbonylaMino)pyridin-4-ylboronic acid
CAS Number: 903513-59-7
Product Number: AG00GX46(AGN-00GWYM)
Synonyms:
MDL No:
Molecular Formula: C10H15BN2O4
Molecular Weight: 238.0481

Identification/Properties

Computed Properties
Molecular Weight:
238.05g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
238.112g/mol
Monoisotopic Mass:
238.112g/mol
Topological Polar Surface Area:
91.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
268
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


2-(tert-Butoxycarbonylamino)pyridin-4-ylboronic acid is a versatile chemical compound that finds applications in various chemical syntheses. With its boronic acid functionality, this compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic method allows for the formation of carbon-carbon bonds under mild conditions, making it an indispensable tool in the arsenal of organic chemists. Furthermore, the presence of the pyridine ring in the molecule imparts unique properties, making it useful in the construction of heterocyclic compounds. This enables the synthesis of a wide range of complex molecules with diverse applications in medicinal chemistry, materials science, and other fields.Overall, 2-(tert-Butoxycarbonylamino)pyridin-4-ylboronic acid plays a crucial role in advancing chemical synthesis by facilitating the creation of structurally intricate molecules with precision and efficiency.