thiocarbamate
thumb|right|250px|Chemical formula#General forms for organic compounds|General [[structural formulae of O-organyl (1) and S-organyl (2) thiocarbamates]]
Research
12,396 papers- Mouse pharmacokinetics and metabolism of the phenylurea thiocarbamate NSC 161128.Cancer chemotherapy and pharmacology · 2022
- Masking thiol reactivity with thioamide, thiourea, and thiocarbamate-based MBPs.Chemical communications (Cambridge, England) · 2023
- Dicoumarin with dimethyl thiocarbamate in the fluorescent detecting for Au(3+) in water and cells.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy · 2023
- Thiocarbamate-linked polysulfonate-peptide conjugates as selective hepatocyte growth factor receptor binders.Bioconjugate chemistry · 2014
- Thiocarbamate herbicide-inducible nonheme haloperoxidase of Rhodococcus erythropolis NI86/21.Applied and environmental microbiology · 1997
via PubMed
~2 min read
Article
6 sectionsContents
- Synthesis
- Reactions
- Occurrence
- Uses
- See also
- References
thumb|right|250px|Chemical formula#General forms for organic compounds|General [[structural formulae of O-organyl (1) and S-organyl (2) thiocarbamates]]
In organic chemistry, thiocarbamates (thiourethanes) are a family of organosulfur compounds. As the prefix thio- suggests, they are sulfur analogues of carbamates. There are two isomeric forms of thiocarbamates: O-thiocarbamates, (esters), and S-thiocarbamates, (thioesters).