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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-Dioxaborinane, 2-(2-methoxyphenyl)-

COc1ccccc1B1OCCCO1 Request for Quotation
Chemical Name: 1,3,2-Dioxaborinane, 2-(2-methoxyphenyl)-
CAS Number: 141522-26-1
Product Number: AG001GIJ(AGN-PC-003YHA)
Synonyms:
MDL No:
Molecular Formula: C10H13BO3
Molecular Weight: 192.0194

Identification/Properties

Computed Properties
Molecular Weight:
192.021g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
192.096g/mol
Monoisotopic Mass:
192.096g/mol
Topological Polar Surface Area:
27.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
171
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


2-(2-Methoxyphenyl)-1,3,2-dioxaborinane is a versatile boron-containing compound widely utilized in chemical synthesis as a valuable building block. Its unique structural characteristics make it an essential reagent for various reactions, especially in the field of organic chemistry.Due to its boron functionality, 2-(2-Methoxyphenyl)-1,3,2-dioxaborinane is commonly employed as a boron source in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool in organic synthesis for forming carbon-carbon bonds, making it crucial in the construction of complex organic molecules. The compound's presence enables efficient and selective coupling reactions, leading to the development of new pharmaceuticals, agrochemicals, and materials.Additionally, 2-(2-Methoxyphenyl)-1,3,2-dioxaborinane can participate in palladium-catalyzed allylic substitution reactions, enabling the introduction of diverse functional groups into organic molecules. This versatility expands its application in designing and synthesizing novel chemical structures with tailored properties for specific applications.In summary, the strategic use of 2-(2-Methoxyphenyl)-1,3,2-dioxaborinane in chemical synthesis facilitates the efficient construction of complex organic compounds, driving advancements in various scientific fields and industries.