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CAS 1375301-93-1

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4,4,5,5-Tetramethyl-2-[2-methyl-6-(1-methylethyl)phenyl]-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-[2-methyl-6-(1-methylethyl)phenyl]-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon framework. This compound typically exhibits a high degree of stability due to the presence of the boron-oxygen bond, making it useful in various chemical applications, particularly in organic synthesis and as a reagent in cross-coupling reactions. The presence of multiple methyl groups contributes to its steric bulk, which can influence its reactivity and solubility in organic solvents. Additionally, the aromatic substituent enhances its electronic properties, potentially making it a candidate for applications in materials science or pharmaceuticals. Its specific interactions and reactivity patterns can be further explored in the context of catalysis or as a building block in complex organic molecules. Safety data and handling precautions should be considered, as with all chemical substances, to ensure proper laboratory practices.
Formula:C16H25BO2
InChI:InChI=1S/C16H25BO2/c1-11(2)13-10-8-9-12(3)14(13)17-18-15(4,5)16(6,7)19-17/h8-11H,1-7H3
InChI key:InChIKey=SMLDFHNYBARLNG-UHFFFAOYSA-N
SMILES:C(C)(C)C1=C(C(C)=CC=C1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[2-methyl-6-(1-methylethyl)phenyl]-
  • 4,4,5,5-Tetramethyl-2-[2-methyl-6-(1-methylethyl)phenyl]-1,3,2-dioxaborolane
  • 4,4,5,5-tetramethyl-2-(2-methyl-6-propan-2-ylphenyl)-1,3,2-dioxaborolane
  • 2-(2-isopropyl-6-Methylphenyl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
  • (2-ISOPROPYL-6-METHYLPHENYL)BORONIC ACID PINACOL ESTER
  • (2-ISOPROPYL-6-METHYLPHENYL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE
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