1. Home
  2. (4-butoxy-3-chlorophenyl)boronic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

(4-butoxy-3-chlorophenyl)boronic acid

CCCCOc1ccc(cc1Cl)B(O)O Request for Quotation
Chemical Name: (4-butoxy-3-chlorophenyl)boronic acid
CAS Number: 480438-55-9
Product Number: AG003BV2(AGN-PC-0LOD13)
Synonyms:
MDL No:
Molecular Formula: C10H14BClO3
Molecular Weight: 228.4804

Identification/Properties

Properties
MP:
147-151 °C(lit.)
BP:
376.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
228.479g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
228.072g/mol
Monoisotopic Mass:
228.072g/mol
Topological Polar Surface Area:
49.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
180
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

Request for Quotation

Customer Feedback

Chemical Structure


(4-Butoxy-3-chlorophenyl)boronic acid is a versatile compound commonly utilized in chemical synthesis. With its unique properties, this boronic acid derivative plays a crucial role in various organic reactions, particularly in the field of pharmaceuticals and agrochemicals.In chemical synthesis, (4-Butoxy-3-chlorophenyl)boronic acid is frequently employed as a valuable building block for the construction of complex organic molecules. Its boronic acid moiety allows for the formation of stable boronate esters, which are essential intermediates in Suzuki-Miyaura cross-coupling reactions. This versatile cross-coupling reaction enables the creation of carbon-carbon bonds, facilitating the synthesis of a wide range of biologically active compounds.Additionally, the butoxy and chloro substituents on the phenyl ring provide specific steric and electronic effects, influencing the reactivity and selectivity of the compound in different chemical transformations. These unique structural characteristics make (4-Butoxy-3-chlorophenyl)boronic acid a valuable tool for chemists seeking to design and synthesize novel molecules with tailored properties.Overall, the strategic incorporation of (4-Butoxy-3-chlorophenyl)boronic acid in chemical synthesis offers synthetic chemists a powerful tool for the efficient and selective construction of complex organic structures, making it an indispensable reagent in the realm of modern organic chemistry.