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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, (4-hexylphenyl)-

CCCCCCc1ccc(cc1)B(O)O Request for Quotation
Chemical Name: Boronic acid, (4-hexylphenyl)-
CAS Number: 105365-50-2
Product Number: AG00341T(AGN-PC-0L71V8)
Synonyms:
MDL No: MFCD04039029
Molecular Formula: C12H19BO2
Molecular Weight: 206.0891

Identification/Properties

Properties
BP:
342.6°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
206.092g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
6
Exact Mass:
206.148g/mol
Monoisotopic Mass:
206.148g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
154
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


4-Hexylphenylboronic Acid, known for its versatile application in chemical synthesis, serves as a valuable building block in the field of organic chemistry. With its unique structure and reactivity, this compound plays a crucial role in the formation of carbon-carbon bonds through various coupling reactions.One prominent application of 4-Hexylphenylboronic Acid lies in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for the synthesis of biaryl compounds. By reacting with aryl halides or pseudohalides in the presence of a palladium catalyst, this compound facilitates the construction of complex organic molecules with high efficiency and selectivity.Furthermore, 4-Hexylphenylboronic Acid can also participate in other important transformations, such as Chan-Lam coupling, borylation reactions, and Heck reactions, expanding its utility in the synthesis of pharmaceuticals, agrochemicals, and materials science.Overall, the strategic incorporation of 4-Hexylphenylboronic Acid into synthetic pathways enables chemists to access a diverse array of structurally intricate compounds, making it a valuable tool for advancing the frontiers of chemical research and development.