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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)-

4,4,5,5-tetramethyl-2-(3-phenylphenyl)-1,3,2-dioxaborolane

CC1(C)OB(OC1(C)C)c1cccc(c1)c1ccccc1 Request for Quotation
Chemical Name: 4,4,5,5-tetramethyl-2-(3-phenylphenyl)-1,3,2-dioxaborolane
CAS Number: 912844-88-3
Product Number: AG00GSY4(AGN-PC-01N4XA)
Synonyms:
MDL No:
Molecular Formula: C18H21BO2
Molecular Weight: 280.1691

Identification/Properties

Computed Properties
Molecular Weight:
280.174g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
280.163g/mol
Monoisotopic Mass:
280.163g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
344
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


2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a highly versatile compound that finds extensive applications in chemical synthesis. This unique boron-containing compound is particularly valued in organic synthesis for its ability to serve as a key building block in the creation of various organic molecules.One prominent use of 2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, allows for the selective construction of complex organic structures by combining the boron atom in the dioxaborolane with an organic halide or pseudohalide.Additionally, this compound is instrumental in the synthesis of functional materials, pharmaceuticals, agrochemicals, and advanced materials due to its stability, reactivity, and compatibility with various reaction conditions. Its presence in the synthetic chemist's toolbox enables the efficient and strategic creation of diverse molecular structures with tailored properties and functionalities.