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CAS 749885-71-0

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rel-4,4,5,5-Tetramethyl-2-[(1R,2R)-2-phenylcyclopropyl]-1,3,2-dioxaborolane

Description:
Rel-4,4,5,5-Tetramethyl-2-[(1R,2R)-2-phenylcyclopropyl]-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound is notable for its chirality, as indicated by the (1R,2R) configuration, which contributes to its potential applications in asymmetric synthesis and catalysis. The presence of the phenylcyclopropyl group enhances its steric and electronic properties, making it a valuable intermediate in organic synthesis. The tetramethyl substituents provide increased stability and solubility, which can be advantageous in various chemical reactions. Additionally, compounds like this one are often explored for their utility in medicinal chemistry and materials science due to their unique reactivity and ability to form stable complexes with other molecules. Overall, rel-4,4,5,5-Tetramethyl-2-[(1R,2R)-2-phenylcyclopropyl]-1,3,2-dioxaborolane exemplifies the diverse applications of boron compounds in modern chemistry.
Formula:C15H21BO2
InChI:InChI=1/C15H21BO2/c1-14(2)15(3,4)18-16(17-14)13-10-12(13)11-8-6-5-7-9-11/h5-9,12-13H,10H2,1-4H3/t12-,13+/s2
InChI key:InChIKey=UANSPBMADSQCLG-QWAQRTLVNA-N
SMILES:CC1(C)OB([C@H]2[C@@H](C2)C3=CC=CC=C3)OC1(C)C
Synonyms:
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(1R,2R)-2-phenylcyclopropyl]-, rel-
  • rel-4,4,5,5-Tetramethyl-2-[(1R,2R)-2-phenylcyclopropyl]-1,3,2-dioxaborolane
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90
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