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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-(cyclopropylmethoxy)-5-methylphenyl]boronic acid

Cc1cc(OCC2CC2)cc(c1)B(O)O Request for Quotation
Chemical Name: [3-(cyclopropylmethoxy)-5-methylphenyl]boronic acid
CAS Number: 1256345-78-4
Product Number: AG000O11(AGN-PC-09PYXP)
Synonyms:
MDL No:
Molecular Formula: C11H15BO3
Molecular Weight: 206.0460

Identification/Properties

Computed Properties
Molecular Weight:
206.048g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
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:
206
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


The (3-(Cyclopropylmethoxy)-5-methylphenyl)boronic acid is a versatile compound widely utilized in chemical synthesis as a key building block in the formation of various organic molecules. Its unique structural properties make it an essential tool in the development of pharmaceuticals, agrochemicals, and materials science. In chemical synthesis, this boronic acid derivative serves as a valuable reagent for Suzuki-Miyaura cross-coupling reactions, providing a method for the introduction of the (3-(Cyclopropylmethoxy)-5-methylphenyl) group into target molecules. This reaction enables the formation of complex organic structures by coupling the boronic acid with suitable partners under mild reaction conditions. Furthermore, the presence of the boronic acid moiety in the molecule offers the potential for further functionalization through various transformations such as oxidation, reduction, and substitution reactions. This capability enhances the versatility of the compound in creating diverse chemical entities with tailored properties.Overall, the (3-(Cyclopropylmethoxy)-5-methylphenyl)boronic acid plays a crucial role in advancing the field of chemical synthesis by enabling the efficient construction of complex organic compounds with diverse applications in various industries.