| Weight | 198.221 g/mol |
|---|---|
| Formula | C13H10O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 3 |
4-Phenoxybenzaldehyde (67-36-7)
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- Solvent dependent study of carbonyl vibrations of 3phenoxybenzaldehyde and 4ethoxybenzaldehyde by Raman spectroscopy and ab initio calculations (Journal of Raman Spectroscopy, 2009)
- [Studies on chemotherapeutics for Mycobacterium tuberculosis. XXIV. Synthesis and antibacterial activity of Mycobacterium tuberculosis of 3-methoxy-2-phenoxybenzaldehyde, 3-methoxy-4-(3-methoxyphenoxy) benzaldehyde and 3-methoxy-4-(4-methoxyphenoxy) benzaldehyde derivatives]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1969)
- Electrochemical and chemical oxidation of alcohols in a two-phase system using N-oxopiperidinium salt: Synthesis of 4-chlorobutanal, formylcyclopropanes, andm-phenoxybenzaldehyde (Russian Chemical Bulletin, 1992)
- (24) : 3-Methoxy-2-phenoxybenzaldehyde, 3-Methoxy-4-(3-methoxyphenoxy)benzaldehyde 3-Methoxy-4-(4-methoxyphenoxy) benzaldehyde (1969)
- Simultaneous derivatization/pre-concentration of 3-phenoxybenzaldehyde as transformation product of permethrin with 2,4-dinitrophenylhydrazine by solid phase extraction and spectrophotometric detection (Journal of Analytical Chemistry, 2015)
- ChemInform Abstract: NOxopiperidinium SaltAssisted Electrochemical and Chemical Oxidation of Alcohols in a TwoPhase System: Synthesis of 4Chlorobutanal, Formylcyclopropanes, and mPhenoxybenzaldehyde. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC=C(C=C1)OC2=CC=C(C=C2)C=O
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InChIKeyQWLHJVDRPZNVBS-UHFFFAOYSA-N
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