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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)-

Boronic acid, [2-(phenylmethoxy)phenyl]-

OB(c1ccccc1OCc1ccccc1)O Request for Quotation
Chemical Name: Boronic acid, [2-(phenylmethoxy)phenyl]-
CAS Number: 190661-29-1
Product Number: AG002EPH(AGN-PC-0KKVAS)
Synonyms:
MDL No: MFCD01632206
Molecular Formula: C13H13BO3
Molecular Weight: 228.0515

Identification/Properties

Properties
MP:
105-110 °C(lit.)
BP:
428.7°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
228.054g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
228.096g/mol
Monoisotopic Mass:
228.096g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
217
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:
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-(Benzyloxy)phenyl)boronic acid, commonly used in chemical synthesis, serves as a versatile building block in organic reactions. This compound is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a powerful method for forming carbon-carbon bonds under mild conditions. By incorporating (2-(Benzyloxy)phenyl)boronic acid into the reaction mixture, chemists can efficiently construct complex molecular structures with high selectivity. Additionally, this boronic acid derivative can participate in various transformations, such as direct arylation and borylation reactions, expanding its utility in organic synthesis. Its unique reactivity and compatibility with a wide range of functional groups make it a valuable tool for designing and accessing novel organic compounds.