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CAS 913836-26-7

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

Description:
2-(4-Chloro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boron-containing organic compound characterized by its unique dioxaborolane structure, which features a five-membered ring containing boron and oxygen atoms. This compound is notable for its incorporation of a chloro and nitro substituent on the phenyl ring, which can influence its reactivity and potential applications in organic synthesis. The presence of the tetramethyl groups enhances the stability of the dioxaborolane ring and may affect its solubility and interaction with other chemical species. Typically, compounds like this are utilized in various fields, including medicinal chemistry and materials science, due to their ability to participate in cross-coupling reactions and serve as intermediates in the synthesis of more complex molecules. Additionally, the specific arrangement of substituents can impart unique electronic properties, making it a subject of interest for further research in chemical reactivity and functionalization.
Formula:C12H15BClNO4
InChI:InChI=1S/C12H15BClNO4/c1-11(2)12(3,4)19-13(18-11)8-5-6-9(14)10(7-8)15(16)17/h5-7H,1-4H3
InChI key:InChIKey=VEIRGLFECZUCTI-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(N(=O)=O)=C(Cl)C=C2
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(4-chloro-3-nitrophenyl)-4,4,5,5-tetramethyl-
  • 2-(4-Chloro-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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