4-Benzyloxy-3-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
4-Benzyloxy-3-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

4-Benzyloxy-3-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals

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Quantity:
25 g
100 g
Catalog number A14716.14
also known as A14716-14
Price (USD)/ Each
59.50
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Quantity:
25 g
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Price (USD)/ Each
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4-Benzyloxy-3-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog numberA14716.14
Price (USD)/ Each
59.50
-
Add to cart
Chemical Identifiers
CAS2426-87-1
IUPAC Name4-(benzyloxy)-3-methoxybenzaldehyde
Molecular FormulaC15H14O3
InChI KeyJSHLOPGSDZTEGQ-UHFFFAOYSA-N
SMILESCOC1=CC(C=O)=CC=C1OCC1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Melting Point (clear melt)59.0-66.0?C
Assay (GC)≥97.5%
Appearance (Color)White to pale yellow
FormCrystals or powder or crystalline powder
Free acid (titration)≤1%
4-Benzyloxy-3-methoxybenzaldehyde was used in the synthesis of 1,2-bis(4-benzyloxy-3-methoxyphenyl)-3-hydroxy-propionic acid1. It was also used in first enantioselective total synthesis of a neurotrophic (-)-talaumidin. 4-Benzyloxy-3-methoxybenzaldehyde reacts with benzohydrazide to yield (E)-N?-(4-benzyloxy-3-methoxybenzylidene)benzohydrazide.

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
4-Benzyloxy-3-methoxybenzaldehyde was used in the synthesis of 1,2-bis(4-benzyloxy-3-methoxyphenyl)-3-hydroxy-propionic acid1. It was also used in first enantioselective total synthesis of a neurotrophic (-)-talaumidin. 4-Benzyloxy-3-methoxybenzaldehyde reacts with benzohydrazide to yield (E)-N′-(4-benzyloxy-3-methoxybenzylidene)benzohydrazide.

Solubility
Soluble in chloroform, methanol.

Notes
Air Sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from strong oxidizing agents and strong bases.
RUO – Research Use Only

General References:

  1. J Shi. (E)-N'-(4-Benzyloxy-3-methoxybenzylidene) isonicotinohydrazide. Acta Crystallographica Section E: Structure Reports. 2005E61 (2), 3933-3934.
  2. T Hashimoto.; K Hasegawa.; H Yamaguchi.; M Saito. Structure and synthesis of batatasins, dormancy-inducing substances of yam bulbils. Phytochemistry. 197413 (12), 2849-2852.