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CAS 68716-51-8

:

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

Description:
2-(3,5-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, with the CAS number 68716-51-8, is a boron-containing organic compound characterized by its unique dioxaborolane structure. This compound features a boron atom bonded to two oxygen atoms and a phenyl group substituted with two chlorine atoms at the 3 and 5 positions, along with four methyl groups attached to the boron. The presence of the dichlorophenyl moiety contributes to its potential biological activity and reactivity, while the tetramethyl groups enhance its stability and solubility in organic solvents. Typically, compounds of this nature are utilized in organic synthesis, particularly in cross-coupling reactions, due to the reactivity of the boron atom. Additionally, the compound may exhibit interesting properties such as fluorescence or specific interactions with biological targets, making it of interest in medicinal chemistry and materials science. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or environmental impact.
Formula:C12H15BCl2O2
InChI:InChI=1/C12H15BCl2O2/c1-11(2)12(3,4)17-13(16-11)8-5-9(14)7-10(15)6-8/h5-7H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2cc(cc(c2)Cl)Cl)O1
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(3,5-dichlorophenyl)-4,4,5,5-tetramethyl-
  • 3,5-Dichlorophenylboronic acid pinacol ester
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