| Weight | 101.13 g/mol |
|---|---|
| Formula | C3H3NOS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Isothiazol-3(2H)-one (1003-07-2)
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- Inhibition of Dengue virus and West Nile virus proteases by click chemistry-derived benz[d]isothiazol-3(2H)-one derivatives. (Bioorganic & Medicinal Chemistry, 2012)
- Tilcotil Studies [3+2] additions with isothiazol-3(2H)-one 1,1-dioxide (Helvetica Chimica Acta, 1989)
- Triphenyltin derivatives of isothiazol-3(2H)-one 1,1-dioxides. Synthesis, Mssbauer spectra, some fungitoxicity data, and crystal structure of triphenylstannyl 1,2-benziosthiazol-3-(2H)-one 1,1-dioxideN,N-dimethylformamide (Journal of Organometallic Chemistry, 1991)
- Copper-catalysed one-pot synthesis of N-substituted benzo[d]isothiazol-3(2H)-ones via C-S/N-S bond formation (RSC Advances, 2012)
- 1,3-Dipolar cycloaddition reactions of isothiazol-3(2H)-ones with nitrile oxides. An unexpected site selectivity of the carbonyl bond of 5-benzoyl-isothiazol-3(2H)-one (Journal of Heterocyclic Chemistry, 1996)
- Triphenylstannyl derivatives of isothiazol-3(2H)-one 1,1-dioxides. Crystal structures of 2-triphenylstannyl 1,2-benzisothiazol-3(2H)-one 1,1-dioxide [(C6H5)3SnNC(O)C6H4SO2] and 2-triphenylstannyl 4,5-dimethylisothiazol-3(2H)-one 1,1-dioxide [(C6H5)3SnNC(O)C(CH3)C(CH3)SO2] (Journal of Organometallic Chemistry, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CSNC1=O
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InChIKeyMGIYRDNGCNKGJU-UHFFFAOYSA-N
- Pubchem - Isothiazol-3(2H)-one
- Wikipedia - isothiazolinone
Isothiazolinone is a heterocyclic chemical compound. Derivatives of isothiazolinone are used as biocides, including: Methylisothiazolinone (MIT, MI) Chloromethylisothiazolinone (CMIT, CMI, MCI) Benzisothiazolinone (BIT) Octylisothiazolinone (OIT, OI) Dichlorooctylisothiazolinone (DCOIT, DCOI) Butylbenzisothiazolinone (BBIT)
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