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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)-

[4-(4-butylphenyl)-2-fluorophenyl]boronic acid

CCCCc1ccc(cc1)c1ccc(c(c1)F)B(O)O Request for Quotation
Chemical Name: [4-(4-butylphenyl)-2-fluorophenyl]boronic acid
CAS Number: 1400809-84-8
Product Number: AG001C0K(AGN-PC-07XTG2)
Synonyms:
MDL No:
Molecular Formula: C16H18BFO2
Molecular Weight: 272.1223

Identification/Properties

Computed Properties
Molecular Weight:
272.1g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
272.138388g/mol
Monoisotopic Mass:
272.138388g/mol
Topological Polar Surface Area:
40.5Ų
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
280
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:
H302-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


The (4'-Butyl-3-fluoro-[1,1'-biphenyl]-4-yl)boronic acid is a versatile compound used in chemical synthesis as a key building block in the formation of complex organic molecules. This boronic acid derivative acts as a vital intermediate in the construction of various pharmaceuticals, agrochemicals, and materials due to its ability to participate in a range of cross-coupling reactions. Its unique structure and reactivity allow for efficient and selective functionalization of organic molecules, enabling the creation of new compounds with desirable properties. This compound plays a crucial role in the development of novel drug candidates, advanced materials, and fine chemicals through its application in organic synthesis strategies.