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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)-

(2,4-dichloro-5-phenylmethoxyphenyl)boronic acid

Clc1cc(Cl)c(cc1OCc1ccccc1)B(O)O Request for Quotation
Chemical Name: (2,4-dichloro-5-phenylmethoxyphenyl)boronic acid
CAS Number: 1256346-47-0
Product Number: AG000O21(AGN-PC-09PZ18)
Synonyms:
MDL No:
Molecular Formula: C13H11BCl2O3
Molecular Weight: 296.9416

Identification/Properties

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 Boronic acid, B-[2,4-dichloro-5-(phenylmethoxy)phenyl]- is a versatile chemical reagent widely used in organic synthesis. In chemical synthesis, Boronic acids are known for their ability to form stable covalent bonds with diols, amines, alcohols, and other organic compounds. This specific Boronic acid derivative is particularly valuable in coupling reactions for the synthesis of biaryl compounds, a key structural motif found in various pharmaceuticals, agrochemicals, and materials. Its unique structure featuring dichloro and phenylmethyl ether functionalities imparts specific reactivity that can be utilized in Suzuki-Miyaura cross-coupling reactions to construct complex organic molecules efficiently. Additionally, the presence of these substituents can influence the regioselectivity and reaction rates, making it a valuable tool for fine-tuning synthetic pathways.