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CAS 5553-32-2

:

3-Thiophenamine, tetrahydro-N-2-propen-1-yl-, 1,1-dioxide, hydrochloride (1:1)

Description:
3-Thiophenamine, tetrahydro-N-2-propen-1-yl-, 1,1-dioxide, hydrochloride (1:1), with the CAS number 5553-32-2, is a chemical compound characterized by its thiophene ring structure, which contributes to its aromatic properties. The presence of the tetrahydro group indicates that it has a saturated cyclic structure, while the N-2-propen-1-yl substituent suggests it has an alkene functionality that may participate in various chemical reactions. The 1,1-dioxide designation indicates the presence of two oxygen atoms bonded to the sulfur atom in the thiophene ring, enhancing its reactivity and solubility in polar solvents. As a hydrochloride salt, it is typically more stable and soluble in aqueous solutions, making it suitable for various applications in pharmaceuticals and organic synthesis. The compound may exhibit biological activity, potentially serving as a precursor or intermediate in the synthesis of more complex molecules. Its specific properties, such as melting point, solubility, and reactivity, would depend on the conditions under which it is handled and utilized.
Formula:C7H13NO2S·ClH
InChI:InChI=1S/C7H13NO2S.ClH/c1-2-4-8-7-3-5-11(9,10)6-7;/h2,7-8H,1,3-6H2;1H
InChI key:InChIKey=WKPLATIOZRZXOQ-UHFFFAOYSA-N
SMILES:N(CC=C)C1CS(=O)(=O)CC1.Cl
Synonyms:
  • 3-[(Prop-2-en-1-yl)amino]-1λ6-thiolane-1,1-dione hydrochloride
  • 3-Thiophenamine, tetrahydro-N-2-propenyl-, 1,1-dioxide, hydrochloride
  • 3-Thiophenamine, N-allyltetrahydro-, 1,1-dioxide, hydrochloride
  • 3-Thiophenamine, tetrahydro-N-2-propen-1-yl-, 1,1-dioxide, hydrochloride (1:1)
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