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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)-

(3-bromo-6-fluoro-2-methoxyphenyl)boronic acid

COc1c(Br)ccc(c1B(O)O)F Request for Quotation
Chemical Name: (3-bromo-6-fluoro-2-methoxyphenyl)boronic acid
CAS Number: 957120-30-8
Product Number: AG006BL6(AGN-PC-078TE4)
Synonyms:
MDL No: MFCD09475911
Molecular Formula: C7H7BBrFO3
Molecular Weight: 248.8421

Identification/Properties

Properties
BP:
349.7°C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
248.842g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
247.966g/mol
Monoisotopic Mass:
247.966g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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


The B-(3-Bromo-6-fluoro-2-methoxyphenyl)boronic acid is a versatile compound commonly utilized in chemical synthesis as a key building block. Its unique structure and reactivity make it a valuable tool for the creation of various organic compounds and pharmaceutical intermediates. This boronic acid derivative serves as a crucial component in Suzuki-Miyaura cross-coupling reactions, enabling the formation of complex molecular structures with high efficiency and selectivity. Moreover, its substituent groups facilitate diverse functionalization strategies, allowing for the rapid assembly of intricate molecular architectures. In the realm of medicinal chemistry, this compound plays a vital role in the synthesis of novel drug candidates and bioactive molecules, showcasing its significance in the development of cutting-edge therapeutics. By incorporating B-(3-Bromo-6-fluoro-2-methoxyphenyl)boronic acid into synthetic pathways, chemists can access a wide array of chemical transformations, paving the way for innovation and progress in the field of organic synthesis.