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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, (2-cyclohexylethyl)-

OB(CCC1CCCCC1)O Request for Quotation
Chemical Name: Boronic acid, (2-cyclohexylethyl)-
CAS Number: 105869-43-0
Product Number: AG008U3S(AGN-PC-073081)
Synonyms:
MDL No:
Molecular Formula: C8H17BO2
Molecular Weight: 156.0304

Identification/Properties

Computed Properties
Molecular Weight:
156.032g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
156.132g/mol
Monoisotopic Mass:
156.132g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
100
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(cyclohexylethyl)boronic acid is a versatile and important reagent in chemical synthesis due to its unique boronic acid functionality. This compound is commonly used in organic chemistry reactions as a key building block for constructing complex molecules. In organic synthesis, 2-(cyclohexylethyl)boronic acid participates in a variety of reactions, most notably in Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl or vinyl boronic acid with an aryl or vinyl halide or pseudohalide in the presence of a palladium catalyst. The resulting product is a biaryl or bivinyl compound, which is crucial in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, 2-(cyclohexylethyl)boronic acid can also be utilized in various transformations such as direct C-H functionalization, borylation, and Suzuki-Miyaura polycondensation. These transformations enable the rapid and efficient construction of molecular scaffolds with high selectivity and efficiency.Overall, the application of 2-(cyclohexylethyl)boronic acid in chemical synthesis plays a significant role in the development of new molecules with diverse functionalities and applications.