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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)-

Boronicacid, B-(5-formyl-3-pyridinyl)-

O=Cc1cncc(c1)B(O)O Request for Quotation
Chemical Name: Boronicacid, B-(5-formyl-3-pyridinyl)-
CAS Number: 919347-69-6
Product Number: AG00675S(AGN-PC-07HB0U)
Synonyms:
MDL No:
Molecular Formula: C6H6BNO3
Molecular Weight: 150.9277

Identification/Properties

Properties
BP:
399°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
150.928g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
151.044g/mol
Monoisotopic Mass:
151.044g/mol
Topological Polar Surface Area:
70.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
142
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

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


Utilizing (5-Formylpyridin-3-yl)boronic acid in chemical synthesis offers a versatile approach to introducing the aldehyde functional group into organic molecules. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and compatibility with a wide range of reaction conditions. In organic synthesis, (5-Formylpyridin-3-yl)boronic acid can undergo various transformations such as cross-coupling reactions, Suzuki-Miyaura couplings, and palladium-catalyzed coupling reactions to form complex structures with high efficiency. Its ability to act as a multifunctional intermediate enables chemists to access diverse chemical space, making it an indispensable tool in the development of novel compounds and materials.