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CAS 1309982-17-9

:

2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine

Description:
2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine is an organic compound characterized by the presence of a chloro group and an amine functional group on a benzene ring, along with a boron-containing dioxaborolane moiety. The compound features a chlorinated aromatic system, which can influence its reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions. The dioxaborolane group is notable for its ability to participate in various chemical transformations, including Suzuki coupling, making this compound potentially useful in the development of pharmaceuticals and agrochemicals. Its structure suggests a degree of steric hindrance due to the bulky tetramethyl groups, which may affect its solubility and reactivity. Additionally, the presence of both electron-withdrawing (chlorine) and electron-donating (amine) groups can lead to interesting electronic properties, influencing its behavior in chemical reactions. Overall, this compound exemplifies the complexity and versatility of organoboron chemistry.
Formula:C12H17BClNO2
InChI:InChI=1S/C12H17BClNO2/c1-11(2)12(3,4)17-13(16-11)8-6-5-7-9(14)10(8)15/h5-7H,15H2,1-4H3
InChI key:InChIKey=LQBRFQDRFCWLJV-UHFFFAOYSA-N
SMILES:NC1=C(B2OC(C)(C)C(C)(C)O2)C=CC=C1Cl
Synonyms:
  • 2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenamine
  • 2-Chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
  • Benzenamine, 2-chloro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-Chloro-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)aniline
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