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CAS 741699-27-4

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2-[2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethanol

Description:
2-[2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethanol, with the CAS number 741699-27-4, is a chemical compound characterized by its complex structure, which includes a chloro-substituted phenyl group and a boron-containing moiety. This compound features a dioxaborolane ring, which is known for its stability and utility in organic synthesis, particularly in the formation of boron-containing intermediates. The presence of the phenoxy group suggests potential applications in pharmaceuticals or agrochemicals, as phenolic compounds often exhibit biological activity. Additionally, the hydroxyl group in the ethanol moiety may enhance solubility in polar solvents and facilitate interactions in biological systems. The compound's unique structure may also impart specific reactivity patterns, making it a candidate for further chemical transformations. Overall, its characteristics suggest versatility in synthetic applications, particularly in the development of new materials or biologically active compounds.
Formula:C14H20BClO4
InChI:InChI=1S/C14H20BClO4/c1-13(2)14(3,4)20-15(19-13)10-5-6-12(11(16)9-10)18-8-7-17/h5-6,9,17H,7-8H2,1-4H3
InChI key:InChIKey=ACUKCZUDFGZKGV-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(Cl)=C(OCCO)C=C2
Synonyms:
  • 2-[2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethanol
  • 2-[2-Chloro-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethan-1-ol
  • Ethanol, 2-[2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-
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