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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)-

1,3,2-Dioxaborolane, 2-(2-methoxyphenyl)-4,4,5,5-tetramethyl-

COc1ccccc1B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: 1,3,2-Dioxaborolane, 2-(2-methoxyphenyl)-4,4,5,5-tetramethyl-
CAS Number: 190788-60-4
Product Number: AG002ESY(AGN-PC-008DX1)
Synonyms:
MDL No:
Molecular Formula: C13H19BO3
Molecular Weight: 234.0992

Identification/Properties

Computed Properties
Molecular Weight:
234.102g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
234.143g/mol
Monoisotopic Mass:
234.143g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
262
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-(2-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, also known as $name$, is a versatile chemical compound widely utilized in organic synthesis. This boron-containing compound serves as a valuable building block in the formation of various organic molecules, particularly in the field of medicinal chemistry and material science.In chemical synthesis, $name$ is often employed as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions. This powerful and widely utilized reaction allows for the formation of carbon-carbon bonds under mild reaction conditions, making it a popular choice for the creation of complex organic molecules. By participating in the cross-coupling reactions, $name$ can be used to introduce the 2-methoxyphenyl group into target molecules, providing a key structural feature for further modification.Additionally, the unique structure of 2-(2-Methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane imparts stability and selectivity to the reactions in which it is involved, enhancing the efficiency and specificity of the synthetic processes. Its high reactivity and compatibility with various functional groups make it a valuable tool for chemists seeking to design and synthesize new compounds for a wide range of applications.