1. Home
  2. (4-ethoxycarbonyl-3-methoxyphenyl)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-ethoxycarbonyl-3-methoxyphenyl)boronic acid

CCOC(=O)c1ccc(cc1OC)B(O)O Request for Quotation
Chemical Name: (4-ethoxycarbonyl-3-methoxyphenyl)boronic acid
CAS Number: 911312-76-0
Product Number: AG00GT7S(AGN-PC-07XSK0)
Synonyms:
MDL No:
Molecular Formula: C10H13BO5
Molecular Weight: 224.0182

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


The compound (4-(Ethoxycarbonyl)-3-methoxyphenyl)boronic acid is a versatile reagent commonly used in organic chemical synthesis. It serves as a key building block in the preparation of various biologically active compounds, pharmaceuticals, and agrochemicals. This boronic acid derivative is particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely employed method for constructing carbon-carbon bonds. By utilizing this reagent, chemists can selectively introduce the (4-(ethoxycarbonyl)-3-methoxyphenyl) group into their target molecules, enabling the synthesis of complex organic structures with enhanced functionalities. Furthermore, the presence of the boronic acid moiety facilitates its integration into molecular frameworks for further functionalization through diverse chemistry transformations. Its compatibility with a range of reaction conditions and its ability to participate in critical bond-forming processes make it an indispensable tool for organic chemists striving to access new chemical entities and advance the frontiers of chemical synthesis.