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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)-

(7-fluoro-2-methylquinolin-8-yl)boronic acid

Cc1ccc2c(n1)c(B(O)O)c(cc2)F Request for Quotation
Chemical Name: (7-fluoro-2-methylquinolin-8-yl)boronic acid
CAS Number: 1072945-61-9
Product Number: AG003BZ0(AGN-PC-07XTY8)
Synonyms:
MDL No:
Molecular Formula: C10H9BFNO2
Molecular Weight: 204.9934

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
204.995g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
205.071g/mol
Monoisotopic Mass:
205.071g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
230
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


B-(7-Fluoro-2-methyl-8-quinolinyl)boronic acid is a valuable chemical reagent commonly utilized in chemical synthesis processes. Specifically, this compound serves as a versatile building block in the formation of various organic molecules through the Suzuki-Miyaura cross-coupling reaction. By acting as a boronic acid derivative, it can efficiently form carbon-carbon bonds with various aryl halides or pseudohalides under palladium-catalyzed conditions. This reaction is widely employed in the synthesis of pharmaceuticals, agrochemicals, and materials science, making B-(7-Fluoro-2-methyl-8-quinolinyl)boronic acid an essential tool in modern organic chemistry research and development.