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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-butoxyphenyl)-

CCCCOc1ccccc1B(O)O Request for Quotation
Chemical Name: Boronic acid, (2-butoxyphenyl)-
CAS Number: 91129-69-0
Product Number: AG003GTL(AGN-PC-0LMCQX)
Synonyms:
MDL No: MFCD03427052
Molecular Formula: C10H15BO3
Molecular Weight: 194.0353

Identification/Properties

Properties
MP:
69-73°C(lit.)
BP:
351.8 °C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
194.037g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
194.111g/mol
Monoisotopic Mass:
194.111g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
152
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


2-Butoxyphenylboronic acid is a versatile compound widely used in chemical synthesis as a building block for various organic reactions. Its application in Suzuki-Miyaura cross-coupling reactions allows for the efficient formation of carbon-carbon bonds, making it an essential tool in the synthesis of complex organic molecules. Additionally, 2-Butoxyphenylboronic acid can be utilized in the preparation of pharmaceutical intermediates, agrochemicals, and materials science research. Its unique structural properties make it a valuable reagent for the creation of new compounds with diverse functionalities, showcasing its significance in modern organic synthesis methodologies.