| Weight | 108.231 g/mol |
|---|---|
| Formula | C3H8S2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
1,3-Propanedithiol (109-80-8)
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- Synthesis and Chemistry of New Nickel, Palladium, and Platinum Complexes of 1,2-Ethanedithiol, 1,3-Propanedithiol, 1,4-Butanedithiol, 1,4,8-Trithianonane, and 1,4,8,11-Tetrathiaundecane (Inorganic Chemistry, 1976)
- Adsorption Characteristics of 1,3-Propanedithiol on Gold: Surface-Enhanced Raman Scattering and Ellipsometry Study (Journal of Physical Chemistry B, 2000)
- The First Nonthiolic, Odorless 1,3-Propanedithiol Equivalent and Its Application in Thioacetalization. (Journal of Organic Chemistry, 2003)
- Regioselective syntheses of 3-aminomethyl-5-substituted isoxazoles : a facile and chemoselective reduction of azide to amine by sodium borohydride using 1,3-propanedithiol as a catalyst (Tetrahedron Letters, 1993)
- AcidCatalyzed Demetalation of NickelHydrocorphin and CobaltCorrin Complexes with 1,3Propanedithiol (Angewandte Chemie, 1983)
- Condensation reactions of the mononuclear nickel(II) complexes [RN(PPh2)2]NiCl2 with 1,2-ethanedithiol or 1,3-propanedithiol (Inorganica Chimica Acta, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(CS)CS
-
InChIKeyZJLMKPKYJBQJNH-UHFFFAOYSA-N
- Pubchem - 1,3-Propanedithiol
- Wikipedia - 1,3-propane dithiol
1,3-Propanedithiol is the chemical compound with the formula HSCH2CH2CH2SH. This dithiol is a useful reagent in organic synthesis. This liquid, which is readily available commercially, has an intense stench.
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