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CAS 1002727-88-9

:

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman

Description:
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, identified by its CAS number 1002727-88-9, is a chemical compound that features a chroman moiety substituted with a boron-containing group. The presence of the dioxaborolane ring contributes to its unique reactivity and potential applications in organic synthesis, particularly in the formation of carbon-boron bonds. This compound is characterized by its stability under ambient conditions, although it may be sensitive to moisture due to the boron atom. The tetramethyl substituents enhance its lipophilicity, which can influence its solubility in organic solvents. Additionally, the chroman structure imparts potential biological activity, making it of interest in medicinal chemistry. Overall, this compound exemplifies the intersection of boron chemistry and organic synthesis, with implications for the development of new materials and pharmaceuticals.
Formula:C15H21BO3
InChI:InChI=1S/C15H21BO3/c1-14(2)15(3,4)19-16(18-14)12-7-8-13-11(10-12)6-5-9-17-13/h7-8,10H,5-6,9H2,1-4H3
InChI key:InChIKey=NDSHAELUPJMEBM-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C=2C=C3C(=CC2)OCCC3
Synonyms:
  • 2-(3,4-Dihydro-2H-chromen-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2H-1-Benzopyran, 3,4-dihydro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman
  • 2-(Chroman-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3,4-Dihydro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-1-benzopyran
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