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CAS 5565-36-6

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1,4-Benzenediboronic acid bis(neopentyl glycol) cyclic ester

Description:
1,4-Benzenediboronic acid bis(neopentyl glycol) cyclic ester, with the CAS number 5565-36-6, is a chemical compound characterized by its boronic acid functional groups and cyclic ester structure. This compound typically exhibits properties associated with boron-containing compounds, such as the ability to form complexes with diols and other Lewis bases, making it useful in various chemical reactions, particularly in organic synthesis and materials science. The presence of neopentyl glycol in its structure contributes to its solubility and stability, enhancing its utility in polymer chemistry and as a building block for more complex molecules. Additionally, the cyclic ester formation can influence its reactivity and interaction with other chemical species. This compound may also display interesting thermal and mechanical properties, making it suitable for applications in advanced materials. As with many boronic acids, it may participate in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis.
Formula:C16H24B2O4
InChI:InChI=1/C16H24B2O4/c1-15(2)9-19-17(20-10-15)13-5-7-14(8-6-13)18-21-11-16(3,4)12-22-18/h5-8H,9-12H2,1-4H3
InChI key:InChIKey=XDODHEZHZCJSML-UHFFFAOYSA-N
SMILES:CC1(C)COB(c2ccc(cc2)B2OCC(C)(C)CO2)OC1
Synonyms:
  • 1,3,2-Dioxaborinane, 2,2′-(1,4-phenylene)bis[5,5-dimethyl-
  • 1,4-Benzenediboronic acid bis-2,2-dimethyltrimethylene cyclic ester
  • 1,4-Bis(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzene
  • 2,2'-Benzene-1,4-Diylbis(5,5-Dimethyl-1,3,2-Dioxaborinane)
  • 2,2-(1,4-Phenylene)bis(5,5-dimethyl-1,3,2-dioxaborinane)
  • 2-[4-(5,5-Dimethyl-1,3,2-Dioxaborinan-2-Yl)Phenyl]-5,5-Dimethyl-1,3,2-Dioxaborinane
  • p-Benzenediboronic acid, cyclic bis(2,2-dimethyltrimethylene) ester
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