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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)-

(2-(Benzyloxy)-4-bromo-6-fluorophenyl)boronic acid

Brc1cc(OCc2ccccc2)c(c(c1)F)B(O)O Request for Quotation
Chemical Name: (2-(Benzyloxy)-4-bromo-6-fluorophenyl)boronic acid
CAS Number: 1264175-59-8
Product Number: AG000SRT(AGN-PC-0WAMPH)
Synonyms:
MDL No: MFCD12026729
Molecular Formula: C13H11BBrFO3
Molecular Weight: 324.9380

Identification/Properties

Computed Properties
Molecular Weight:
324.94g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
323.997g/mol
Monoisotopic Mass:
323.997g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
277
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2-(Benzyloxy)-4-bromo-6-fluorophenyl)boronic acid is a versatile and valuable compound in chemical synthesis. This boronic acid derivative is commonly utilized in organic chemistry as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and materials.One important application of (2-(Benzyloxy)-4-bromo-6-fluorophenyl)boronic acid is its use in Suzuki-Miyaura cross-coupling reactions. In this widely used synthetic method, the boronic acid moiety of this compound can undergo a palladium-catalyzed coupling reaction with aryl halides or triflates, leading to the formation of biaryl compounds. This reaction allows for the creation of complex molecular structures with high efficiency and selectivity.Furthermore, (2-(Benzyloxy)-4-bromo-6-fluorophenyl)boronic acid can also participate in other types of carbon-carbon and carbon-heteroatom bond-forming reactions, such as Buchwald-Hartwig amination and Stille coupling. By incorporating this boronic acid derivative into synthetic routes, chemists can access a diverse array of functionalized aromatic compounds that are crucial for drug discovery, material science, and other chemical research endeavors.