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CAS 4490-75-9

:

2-(2-Mercaptoethyl)-1H-isoindole-1,3(2H)-dione

Description:
2-(2-Mercaptoethyl)-1H-isoindole-1,3(2H)-dione, also known by its CAS number 4490-75-9, is a chemical compound characterized by its isoindole structure, which features a dione functional group and a mercaptoethyl substituent. This compound typically exhibits properties associated with thiols due to the presence of the mercapto group, which can participate in redox reactions and form disulfide bonds. The isoindole moiety contributes to its potential as a ligand in coordination chemistry and may exhibit biological activity, including antioxidant properties. The compound is likely to be soluble in polar organic solvents, and its reactivity can be influenced by the presence of the thiol group, making it useful in various synthetic applications. Additionally, its unique structure may allow for interactions with biological systems, suggesting potential applications in pharmaceuticals or materials science. Safety data should be consulted for handling and storage, as compounds containing thiol groups can be sensitive to oxidation and may have specific toxicity profiles.
Formula:C10H9NO2S
InChI:InChI=1S/C10H9NO2S/c12-9-7-3-1-2-4-8(7)10(13)11(9)5-6-14/h1-4,14H,5-6H2
InChI key:InChIKey=UHOPWFKONJYLCF-UHFFFAOYSA-N
SMILES:O=C1C=2C(C(=O)N1CCS)=CC=CC2
Synonyms:
  • 1H-Isoindole-1,3(2H)-dione, 2-(2-mercaptoethyl)-
  • 2-(2-Mercaptoethyl)-1H-isoindole-1,3(2H)-dione
  • 2-(2-Mercaptoethyl)isoindoline-1,3-dione
  • 2-(2-Sulfanylethyl)-2,3-dihydro-1H-isoindole-1,3-dione
  • 2-(2-Sulfanylethyl)isoindole-1,3-dione
  • 2-Phthalimidoethanethiol
  • N-(2-Mercaptoethyl)phthalimide
  • NSC 62328
  • Phthalimide, N-(2-mercaptoethyl)-
  • Phthalimidoethanethiol
  • 2-(2-Sulfanylethyl)-1H-isoindole-1,3(2H)-dione
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