| Weight | 212.248 g/mol |
|---|---|
| Formula | C14H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
3-Benzyloxybenzaldehyde (1700-37-4)
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- Copper(II) and nickel(II) complexes of benzyloxybenzaldehyde-4-phenyl-3-thiosemicarbazone: Synthesis, characterization and biological activity (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2010)
- Synthesis, spectral characterization and biological activities of Mn(II) and Co(II) complexes with benzyloxybenzaldehyde-4-phenyl-3-thiosemicarbazone (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- In vivo evaluation of the synthesized novel 2-benzyloxybenzaldehyde analog CCY-1a-E2 for the treatment of leukemia in the BALB/c mouse WEHI-3 allograft model (Oncology Letters, 2013)
- Synthesis, Crystal Structure, Antioxidant, Antimicrobial, and Mutagenic Activities and DNA Interaction Studies of Ni(II) Schiff Base 4-Methoxy-3-benzyloxybenzaldehyde Thiosemicarbazide Complexes (International Scholarly Research Notices, 2013)
- SPECTRAL, STRUCTURAL AND BIOLOGICAL ANALYSIS OF Cr(III) COMPLEX WITH BENZYLOXYBENZALDEHYDE-4-PHENYL-3-THIOSEMICARBAZONE Research Article (2012)
- Synthesis and Characterization of 4-Benzyloxybenzaldehyde-4-methyl-3-thiosemicarbazone (Containing Sulphur and Nitrogen Donor Atoms) and Its Cd(II) Complex (2015)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=CC=C(C=C1)COC2=CC=CC(=C2)C=O
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InChIKeyJAICGBJIBWDEIZ-UHFFFAOYSA-N
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