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CAS 68716-50-7

:

1,3,2-Dioxaborolane, 2-(2,4-dichlorophenyl)-4,4,5,5-tetramethyl-

Description:
1,3,2-Dioxaborolane, 2-(2,4-dichlorophenyl)-4,4,5,5-tetramethyl- is an organoboron compound characterized by its unique dioxaborolane ring structure, which features a five-membered cyclic arrangement containing two oxygen atoms and a boron atom. This compound typically exhibits properties associated with boron-containing compounds, such as potential reactivity in organic synthesis and applications in materials science. The presence of the 2,4-dichlorophenyl group contributes to its hydrophobic characteristics and may influence its electronic properties, making it useful in various chemical reactions, including cross-coupling reactions. The tetramethyl substituents enhance its steric bulk, which can affect its reactivity and solubility in organic solvents. Overall, this compound is of interest in the field of synthetic organic chemistry, particularly for its potential applications in the development of pharmaceuticals and agrochemicals. Safety and handling precautions should be observed due to the presence of chlorine substituents, which may impart toxicity.
Formula:C12H15BCl2O2
InChI:InChI=1S/C12H15BCl2O2/c1-11(2)12(3,4)17-13(16-11)9-6-5-8(14)7-10(9)15/h5-7H,1-4H3
InChI key:InChIKey=SMSBTAPKLZZTAU-UHFFFAOYSA-N
SMILES:ClC1=C(C=CC(Cl)=C1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 2,4-Dichlorobenzeneboronic acid pinacol cyclic ester
  • 1,3-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
  • 1,3,2-Dioxaborolane, 2-(2,4-dichlorophenyl)-4,4,5,5-tetramethyl-
  • 2-(2,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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