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CAS 1256781-74-4

:

2-(2-Chloro-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-(2-Chloro-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique boron-containing dioxaborolane ring structure. This compound features a chlorinated aromatic substituent, which contributes to its potential reactivity and applications in organic synthesis, particularly in cross-coupling reactions. The presence of multiple methyl groups enhances its steric bulk, influencing its solubility and reactivity. The dioxaborolane moiety is known for its ability to form stable complexes with various nucleophiles, making it valuable in the development of boron-based reagents. Additionally, the chlorinated phenyl group may impart specific electronic properties, affecting the compound's behavior in chemical reactions. Overall, this substance is of interest in medicinal chemistry and materials science due to its potential utility in synthesizing complex organic molecules and its role in the development of boron-containing pharmaceuticals. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity and reactivity.
Formula:C14H20BClO2
InChI:InChI=1S/C14H20BClO2/c1-9-7-10(2)12(16)11(8-9)15-17-13(3,4)14(5,6)18-15/h7-8H,1-6H3
InChI key:InChIKey=CNXXDGCVMFEQMM-UHFFFAOYSA-N
SMILES:ClC1=C(B2OC(C)(C)C(C)(C)O2)C=C(C)C=C1C
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(2-chloro-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-
  • 2-(2-Chloro-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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