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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-cyclopentyloxyphenyl)boronic acid

OB(c1cccc(c1)OC1CCCC1)O Request for Quotation
Chemical Name: (3-cyclopentyloxyphenyl)boronic acid
CAS Number: 959850-87-4
Product Number: AG0069NN(AGN-PC-06GMIT)
Synonyms:
MDL No:
Molecular Formula: C11H15BO3
Molecular Weight: 206.0460

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
206.048g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
206.111g/mol
Monoisotopic Mass:
206.111g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
192
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3-(Cyclopentyloxy)phenyl)boronic acid is a versatile compound commonly used in organic chemical synthesis. Its unique structure, consisting of a boronic acid group attached to a phenyl ring with a cyclopentyloxy substituent, lends itself to a variety of applications in the field of chemistry.One of the key uses of (3-(Cyclopentyloxy)phenyl)boronic acid is as a reagent in Suzuki-Miyaura cross-coupling reactions. In this reaction, the boronic acid moiety undergoes a palladium-catalyzed coupling with an aryl or vinyl halide, resulting in the formation of a new carbon-carbon bond. This powerful synthetic method allows for the construction of complex molecular structures with high efficiency and selectivity.Additionally, (3-(Cyclopentyloxy)phenyl)boronic acid can also be employed as a building block in the synthesis of biologically active molecules, pharmaceuticals, and functional materials. By incorporating this compound into the molecular structure of a target compound, chemists can introduce specific functionalities and enhance the desired properties of the final product.Overall, the diverse applications of (3-(Cyclopentyloxy)phenyl)boronic acid make it a valuable tool in the toolbox of synthetic chemists, enabling the efficient and precise construction of complex molecules for various purposes.