| Weight | 124.208 g/mol |
|---|---|
| Formula | C7H8S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
p-Toluenethiol (26445-03-4, 106-45-6)
4-methylbenzenethiol
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- Potential-Induced Structural Change in a Self-Assembled Monolayer of 4-Methylbenzenethiol on Au(111) (Journal of Physical Chemistry C, 2007)
- The Stereochemistry of Base-catalyzed Additions of p-Toluenethiol to Several Negatively-substituted Acetylenes. An Exception to the Rule of trans-Nucleophilic Addition1,2 (Journal of the American Chemical Society, 1957)
- The Stereochemistry of the Base-catalyzed Addition of p-Toluenethiol to Sodium and Ethyl Phenylpropiolate1,2 (Journal of the American Chemical Society, 1959)
- The Stereochemistry of the Base-catalyzed Addition of p-Toluenethiol to Disodium and Diethyl Acetylenedicarboxylate1,2 (Journal of the American Chemical Society, 1959)
- Multilayers of 4-methylbenzenethiol functionalized gold nanoparticles fabricated by Langmuir-Blodgett and Langmuir-Schaefer deposition (Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2006)
- An Efficient Synthesis of 2,6-Disubstituted 2,3-Dihydro-4H-pyran-4-ones via Sonogashira Coupling of p-Toluenethiol Esters (Synlett, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 4-methylbenzenethiol
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SMILESCC1=CC=C(C=C1)S
-
InChIKeyWLHCBQAPPJAULW-UHFFFAOYSA-N
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