| Weight | 150.177 g/mol |
|---|---|
| Formula | C9H10O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
o-Tolyl acetate (533-18-6, 1333-46-6)
cresyl acetate · 4-cresyl acetate · para-cresyl acetate
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- An Evaluation of Cresyl Echt Violet Acetate as a Nissl Stain (Biotechnic & Histochemistry, 1955)
- Spectrophotometric Determination of Bio-Active Compounds in Commercial Samples with Nitrous Acid and Cresyl Fast Violet Acetate (Analytical Letters, 1996)
- Electronic absorption spectra of cresyl violet acetate in anisotropic and isotropic solvents (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2007)
- Reactions of di-o-tolyl telluride and selenide with palladium acetate: isolation of a novel palladium complex of a tellurenic acid anhydride and related trinuclear and tetranuclear palladium complexes (Organometallics, 2011)
- Application of central composite rotatable design to lipase catalysed synthesis of m-cresyl acetate (World Journal of Microbiology & Biotechnology, 2002)
- THE EFFECT OF ACETATE BUFFER MIXTURES, ACETIC ACID, AND SODIUM ACETATE, ON THE PROTOPLASM, AS INFLUENCING THE RATE OF PENETRATION OF CRESYL BLUE INTO THE VACUOLE OF NITELLA (The Journal of General Physiology, 1927)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - cresyl acetate
- 4-cresyl acetate
- para-cresyl acetate
- p-cresyl acetate
-
SMILESCC1=CC=CC=C1OC(=O)C
-
InChIKeyAMZORBZSQRUXNC-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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o-Tolyl acetate
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