CAS 1127-29-3

2,2,4,4-Tetramethyl-1,3-cyclobutanedione 1,3-dioxime

Description:

2,2,4,4-Tetramethyl-1,3-cyclobutanedione 1,3-dioxime, with CAS number 1127-29-3, is a chemical compound characterized by its unique structure, which includes a cyclobutane ring and dioxime functional groups. This compound typically appears as a solid and is known for its potential applications in organic synthesis and coordination chemistry. The presence of the dioxime groups contributes to its chelating properties, allowing it to form complexes with various metal ions. Its tetramethyl substitution enhances its steric hindrance, influencing its reactivity and solubility in organic solvents. The compound is generally stable under standard conditions but may undergo reactions typical of dioximes, such as oxidation or complexation. Safety data indicate that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Overall, 2,2,4,4-Tetramethyl-1,3-cyclobutanedione 1,3-dioxime is a notable compound in the field of organic chemistry, particularly for its structural features and potential applications.

Formula: C₈H₁₄N₂O₂

InChI: InChI=1S/C8H14N2O2/c1-7(2)5(9-11)8(3,4)6(7)10-12/h11-12H,1-4H3

InChI key: InChIKey=HVHSYOQZXWLFGF-UHFFFAOYSA-N

SMILES: N(O)=C1C(C)(C)C(=NO)C1(C)C

Synonyms:

• 1,3-Cyclobutanedione, 2,2,4,4-tetramethyl-, dioxime
• 2,2,4,4-Tetramethyl-1,3-cyclobutanedioxime
• 1,3-Cyclobutanedione, tetramethyl-, dioxime
• 2,2,4,4-Tetramethyl-1,3-cyclobutanedione 1,3-dioxime
• 1,3-Cyclobutanedione, 2,2,4,4-tetramethyl-, 1,3-dioxime