| Weight | 85.131 g/mol |
|---|---|
| Formula | C3H3NS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Isothiazole (288-16-4)
288-16-4
Score:
#2494 in Biochemistry
,
#4876 in Biology
,
#6234 in Chemistry
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LabBot
- Synthesis and biological evaluation of benzo[d]isothiazole, benzothiazole and thiazole Schiff bases. (Bioorganic & Medicinal Chemistry, 2003)
- Synthesis and antiproliferative activity of benzo[d]isothiazole hydrazones (European Journal of Medicinal Chemistry, 2006)
- N-Fluoro-3-cyclohexyl-3-methyl-2,3- dihydrobenzo[1,2-d]isothiazole 1,1-Dioxide: An Efficient Agent for Electrophilic Asymmetric Fluorination of Enolates. (Journal of Organic Chemistry, 1999)
- Thiacyanocarbons. I. Tetracyano-1,4-dithiin, Tetracyanothiophene and Tricyano-1,4-dithiino [c]isothiazole (Journal of the American Chemical Society, 1962)
- Oxazole, isoxazole, thiazole and isothiazole amides (1976)
- Anti-HIV evaluation of benzo[d]isothiazole hydrazones. (European Journal of Medicinal Chemistry, 2009)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 288-16-4
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SMILESC1=CSN=C1
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InChIKeyZLTPDFXIESTBQG-UHFFFAOYSA-N
- Pubchem - Isothiazole
- Wikipedia - isothiazole
An isothiazole, or 1,2-thiazole, is a type of organic compound containing a five-membered aromatic ring that consists of three carbon atoms, one nitrogen atom, and one sulfur atom. Isothiazole is a member of a class of compounds known as azoles. In contrast to the isomeric thiazole, the two heteroatoms are in adjacent positions.
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Areas of Application
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Alternate Names
Estimated Properties
| Boiling Point | 102.25 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 124.84 C | EPI Suite |
| Density | 1.15 g/cm3 | EPA T.E.S.T. |
| Flash Point | 24.87 C | EPA T.E.S.T. |
| Melting Point | -12.35 C | EPI Suite |
| Water Solubility | 14940.7 mg/L | EPA T.E.S.T. |
| Water Solubility | 26539 mg/L | EPI Suite |
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Isothiazole
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