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Thiazoline
Sign in to saveThiazolines (; or dihydrothiazoles) are a group of isomeric 5-membered heterocyclic compounds containing both sulfur and nitrogen in the ring. Although unsubstituted thiazolines are rarely encountered themselves, their derivatives are more common and some are bioactive. For example, in a common post-translational modification, cysteine residues are converted into thiazolines.
Chemical data
- Formula
- C3H5NS
- Molecular weight
- 87.15 g/mol
- IUPAC name
- 4,5-dihydro-1,3-thiazole
- SMILES
- C1CSC=N1
- InChIKey
- CBDKQYKMCICBOF-UHFFFAOYSA-N
- XLogP
- 0.4
- Polar surface area
- 37.7 Ų
- H-bond donors
- 0
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 87.01427
Show 2 more facts
- canonical SMILES
- C1CSC=N1
- chemical formula
- C₃H₅NS
via Wikidata · CC0
~2 min read
Encyclopedic overview
5 sectionsContents
- Isomers
- Synthesis
- Applications
- See also
- References
Thiazolines (; or dihydrothiazoles) are a group of isomeric 5-membered heterocyclic compounds containing both sulfur and nitrogen in the ring. Although unsubstituted thiazolines are rarely encountered themselves, their derivatives are more common and some are bioactive. For example, in a common post-translational modification, cysteine residues are converted into thiazolines.
The name thiazoline originates from the Hantzsch–Widman nomenclature.
Excerpted from Wikipedia’s “Thiazoline” article, available under the CC BY-SA 4.0 licence.
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