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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)-

4-(2,2-Difluoroethoxy)phenylboronic acid

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Chemical Name: 4-(2,2-Difluoroethoxy)phenylboronic acid
CAS Number: 958453-65-1
Product Number: AG00IJHA(AGN-PC-0WAJNS)
Synonyms:
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Molecular Formula:
Molecular Weight:

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Chemical Structure


4-(2,2-DIFLUOROETHOXY)PHENYLBORONIC ACID is a versatile chemical reagent widely utilized in organic synthesis for the preparation of various functional materials. This compound serves as a key building block in the formation of complex organic molecules through Suzuki-Miyaura cross-coupling reactions. By acting as a boronic acid derivative, it enables the selective and efficient formation of carbon-carbon bonds under mild reaction conditions. Additionally, this compound can be employed as a valuable tool in the development of pharmaceuticals, agrochemicals, and materials science due to its ability to introduce the 2,2-difluoroethoxy functional group into target molecules with high precision and control. Furthermore, its unique structural properties make it particularly valuable for the design and synthesis of fluorinated organic compounds, which are of significant interest in medicinal chemistry and materials research.