| Weight | 120.242 g/mol |
|---|---|
| Formula | C4H8S2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,3-Dithiane (505-23-7)
Score:
#6438 in Chemistry
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- Oxidative hydrolysis of 1,3-dithiane derivatives to carbonyl compounds using N-halosuccinimide reagents (Journal of Organic Chemistry, 1971)
- Synthetic uses of the 1,3-dithiane grouping from 1977 to 1988 (Tetrahedron, 1989)
- Stereoelectronic Interactions in Cyclohexane, 1,3-Dioxane, 1,3-Oxathiane, and 1,3-Dithiane: W-Effect, C-X *C-H Interactions, Anomeric EffectWhat Is Really Important? (Journal of Organic Chemistry, 2000)
- Carbanionen der 1,3-Dithiane, Reagentien zur CC-Verknpfung durch nucleophile Substitution oder Carbonyl-Addition (Angewandte Chemie, 1965)
- Silicon-containing carbanions. II. Ketene thioacetal synthesis via 2-lithio-2-trimethylsilyl-1,3-dithiane (Journal of Organic Chemistry, 1972)
- A Convenient Method for Hydrolysis of 1,3-Dithiane Derivatives Using Cupric Chloride (Bulletin of the Chemical Society of Japan, 1972)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CSCSC1
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InChIKeyWQADWIOXOXRPLN-UHFFFAOYSA-N
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1,3-Dithiane
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