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CAS 1218791-20-8

:

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

Description:
2-(4-Ethoxy-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. The presence of the 4-ethoxy-3-nitrophenyl substituent contributes to its chemical reactivity and potential applications in organic synthesis, particularly in the field of medicinal chemistry and materials science. This compound is likely to exhibit properties typical of dioxaborolanes, such as the ability to participate in various chemical reactions, including Suzuki coupling reactions, which are essential for forming carbon-carbon bonds. The nitro group may enhance its electrophilicity, while the ethoxy group can influence solubility and reactivity. Additionally, the tetramethyl substitution on the dioxaborolane ring may affect its stability and steric hindrance. Overall, this compound represents a versatile building block in synthetic organic chemistry, with potential applications in drug development and the creation of functional materials.
Formula:C14H20BNO5
InChI:InChI=1S/C14H20BNO5/c1-6-19-12-8-7-10(9-11(12)16(17)18)15-20-13(2,3)14(4,5)21-15/h7-9H,6H2,1-5H3
InChI key:InChIKey=JDFWXCNRKPGZCO-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(N(=O)=O)=C(OCC)C=C2
Synonyms:
  • 2-(4-Ethoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 2-(4-ethoxy-3-nitrophenyl)-4,4,5,5-tetramethyl-
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