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CAS 51070-56-5

:

N-(Tetrahydro-1,1-dioxido-3-thienyl)glycine

Description:
N-(Tetrahydro-1,1-dioxido-3-thienyl)glycine, with the CAS number 51070-56-5, is an organic compound characterized by its unique structure that includes a thienyl group and a glycine moiety. The presence of the tetrahydro-1,1-dioxide indicates that the compound features a saturated cyclic structure with two oxygen atoms incorporated into the ring, contributing to its reactivity and potential biological activity. This compound is likely to exhibit polar characteristics due to the presence of the amino and carboxylic acid functional groups from the glycine part, which can influence its solubility in water and organic solvents. Additionally, the thienyl ring may impart specific electronic properties and potential interactions with biological systems, making it of interest in medicinal chemistry. Its synthesis and applications could be relevant in various fields, including pharmaceuticals and agrochemicals, although specific applications would depend on further research into its biological activity and stability.
Formula:C6H11NO4S
InChI:InChI=1S/C6H11NO4S/c8-6(9)3-7-5-1-2-12(10,11)4-5/h5,7H,1-4H2,(H,8,9)
InChI key:InChIKey=NLJKAAYXSDTMSI-UHFFFAOYSA-N
SMILES:N(CC(O)=O)C1CS(=O)(=O)CC1
Synonyms:
  • 2-[(1,1-Dioxo-1λ6-thiolan-3-yl)amino]acetic acid
  • 2-[(1,1-Dioxothiolan-3-yl)amino]acetic acid
  • Glycine, N-(tetrahydro-1,1-dioxido-3-thienyl)-
  • Glycine, N-(tetrahydro-3-thienyl)-, S,S-dioxide
  • N-(1,1-dioxidotetrahydrothiophen-3-yl)glycine
  • N-(Tetrahydro-1,1-dioxido-3-thienyl)glycine
  • [(1,1-Dioxidotetrahydrothien-3-yl)amino]acetic acid
  • {[(3R)-1,1-dioxidotetrahydrothiophen-3-yl]ammonio}acetate
  • {[(3S)-1,1-dioxidotetrahydrothiophen-3-yl]ammonio}acetate
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