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CAS 39085-59-1

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2,4,6-Triisopropylbenzenesulfonyl hydrazide

Description:
2,4,6-Triisopropylbenzenesulfonyl hydrazide is an organic compound characterized by its sulfonyl hydrazide functional group, which is known for its reactivity in various chemical transformations. This compound features a triisopropyl-substituted benzene ring, contributing to its hydrophobic nature and potentially influencing its solubility in organic solvents. The presence of the sulfonyl group enhances its ability to participate in nucleophilic reactions, making it useful in synthetic organic chemistry. Additionally, the hydrazide moiety can engage in condensation reactions, forming hydrazones or other derivatives. The compound is typically solid at room temperature and may exhibit moderate stability under standard conditions, although it should be handled with care due to the potential for reactivity. Its applications may include use as a reagent in organic synthesis or as an intermediate in the preparation of more complex molecules. As with many organic compounds, safety precautions should be observed when handling, including the use of appropriate personal protective equipment.
Formula:C15H26N2O2S
InChI:InChI=1S/C15H26N2O2S/c1-9(2)12-7-13(10(3)4)15(20(18,19)17-16)14(8-12)11(5)6/h7-11,17H,16H2,1-6H3
InChI key:InChIKey=UGRVYFQFDZRNMQ-UHFFFAOYSA-N
SMILES:S(NN)(=O)(=O)C1=C(C(C)C)C=C(C(C)C)C=C1C(C)C
Synonyms:
  • (2,4,6-Triisopropylbenzenesulfonyl)hydrazine
  • 2,4,6-Tri(Propan-2-Yl)Benzenesulfonohydrazide
  • 2,4,6-Triisopropylbenzenesulfonic acid hydrazide
  • 2,4,6-Triisopropylbenzenesulfonohydrazide
  • 2,4,6-Triisopropylbenzenesulfonyl hydrazide
  • 2,4,6-Triisopropylphenylsulfonylhydrazine
  • Benzenesulfonic acid, 2,4,6-tris(1-methylethyl)-, hydrazide
  • NSC 620119
  • Trisylhydrazide
  • Trisylhydrazine
  • [(2,4,6-Triisopropylphenyl)sulfonyl] hydrazide
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