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CAS 5231-89-0

:

3,4-Diamino-3-cyclobutene-1,2-dione

Description:
3,4-Diamino-3-cyclobutene-1,2-dione, with the CAS number 5231-89-0, is an organic compound characterized by its unique bicyclic structure, which includes a cyclobutene ring and two amino groups attached to the carbon framework. This compound is notable for its potential applications in organic synthesis and as a precursor in the development of various chemical entities. It typically exhibits properties such as being a solid at room temperature, with a relatively low solubility in non-polar solvents due to its polar functional groups. The presence of the amino groups contributes to its reactivity, allowing it to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the diketone functionality can engage in tautomerization and other reactions typical of carbonyl compounds. Overall, 3,4-Diamino-3-cyclobutene-1,2-dione is of interest in both academic research and potential industrial applications, particularly in the fields of pharmaceuticals and materials science.
Formula:C4H4N2O2
InChI:InChI=1S/C4H4N2O2/c5-1-2(6)4(8)3(1)7/h5-6H2
InChI key:InChIKey=WUACDRFRFTWMHE-UHFFFAOYSA-N
SMILES:NC1=C(N)C(=O)C1=O
Synonyms:
  • 3,4-Diamino-3-cyclobutene-1,2-dione
  • 3-Cyclobutene-1,2-Dione, 3,4-Diamino-
  • Cyclobutenedione, diamino-
  • Squaramide
  • 3,4-Diaminocyclobut-3-ene-1,2-dione
  • diaminocyclobut-3-ene-1,2-dione
  • 1.2-Diaminocyclobuten-3.4-dion
  • 3,4-Dioxocyclobut-1-en-1,2-diamine, 1,2-Diamino-3,4-dioxocyclobut-1-ene
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