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4-Benzyloxy-3-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: A14716.14
25 g, Each
Thermo Scientific Chemicals
4-Benzyloxy-3-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: A14716.14
25 g, Each
Quantity
Catalog number: A14716.14
also known as A14716-14
Price (USD)
Price: 59.50
Online price: 51.65
Your price:
Quantity
-
Chemical Identifiers
CAS
2426-87-1
IUPAC Name
4-(benzyloxy)-3-methoxybenzaldehyde
Molecular Formula
C15H14O3
InChI Key
JSHLOPGSDZTEGQ-UHFFFAOYSA-N
SMILES
COC1=CC(C=O)=CC=C1OCC1=CC=CC=C1
Specifications
Specification SheetAppearance (Color)
White to pale yellow
Form
Crystals or powder or crystalline powder
Melting Point (clear melt)
59.0-66.0?C
Assay (GC)
≥97.5%
Free acid (titration)
≤1%
Description
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.
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
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