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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)-

Pyridine, 3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

CC1(C)OB(OC1(C)C)c1ccc(cc1)c1cccnc1 Request for Quotation
Chemical Name: Pyridine, 3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
CAS Number: 929203-04-3
Product Number: AG00H2TY(AGN-PC-0BS6OJ)
Synonyms:
MDL No:
Molecular Formula: C17H20BNO2
Molecular Weight: 281.1572

Identification/Properties

Computed Properties
Molecular Weight:
281.162g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
281.159g/mol
Monoisotopic Mass:
281.159g/mol
Topological Polar Surface Area:
31.4A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
348
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine plays a crucial role in chemical synthesis as a versatile building block. Its unique structure containing a boronate ester group allows for selective cross-coupling reactions, particularly in Suzuki-Miyaura coupling reactions. This compound serves as a valuable reagent for the formation of carbon-carbon bonds, enabling the efficient synthesis of complex organic molecules. Additionally, its pyridine moiety enhances its reactivity in various transformations, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The utilization of 3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine in chemical synthesis showcases its significance in modern synthetic chemistry and highlights its potential for enabling the construction of intricate molecular structures with precision and efficiency.