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2-Benzyloxybenzaldehyde, 98%
CAS: 5896-17-3 | C14H12O2 | 212.25 g/mol
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Catalog number L12866.18
also known as L12866-18
Price (USD)
98.65
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Online exclusive
Ends: 30-Jun-2026
116.00Save 17.35 (15%)
Each
Quantity:
50 g
Price (USD)
98.65
Special offer
Online exclusive
Ends: 30-Jun-2026
116.00Save 17.35 (15%)
Each
Chemical Identifiers
CAS5896-17-3
IUPAC Name2-(benzyloxy)benzaldehyde
Molecular FormulaC14H12O2
InChI KeyPBEJTRAJWCNHRS-UHFFFAOYSA-N
SMILESO=CC1=CC=CC=C1OCC1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale cream
Assay (GC)≥97.5%
FormCrystalline powder or powder
Free acid (titration)≤1.0%
Melting Point45-50°C
2-Benzyloxybenzaldehyde is used as an organic chemical synthesis intermediate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Benzyloxybenzaldehyde is used as an organic chemical synthesis intermediate.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
2-Benzyloxybenzaldehyde is used as an organic chemical synthesis intermediate.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Jih-Pyang Wang; Ling-Chu Chang, Mei-Feng Hsu; Li-Jiau Huang; Sheng-Chu Kuo. 2-Benzyloxybenzaldehyde inhibits formyl-methionyl-leucyl-phenylalanine stimulation of phospholipase D activation in rat neutrophils. Biochimica et Biophysica Acta (BBA) - General Subjects. 2002, 1573,(1), 26-32.
- Jih-Pyang Wang, Ling-Chu Chang; Yu-Hsiang Kuan; Lo-Ti Tsao; Li-Jiau Huang; Sheng-Chu Kuo. 2-Benzyloxybenzaldehyde inhibits formyl peptide-stimulated increase in intracellular Ca2+ in neutrophils mainly by blocking Ca2+ entry. Naunyn-Schmiedeberg's Archives of Pharmacology. 2004, 370,(5), 353-360.