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2-Hydroxy-5-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: A15753.22
100 g, Each
Thermo Scientific Chemicals
2-Hydroxy-5-methoxybenzaldehyde, 98%, Thermo Scientific Chemicals
Catalog number: A15753.22
100 g, Each
Quantity
Catalog number: A15753.22
also known as A15753-22
Price (USD)
754.00
Each
Quantity
-
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Chemical Identifiers
CAS
672-13-9
IUPAC Name
2-hydroxy-5-methoxybenzaldehyde
Molecular Formula
C8H8O3
InChI Key
FZHSPPYCNDYIKD-UHFFFAOYSA-N
SMILES
COC1=CC=C(O)C(C=O)=C1
Specifications
Specification SheetForm
liquid
Appearance (Color)
Clear, yellow
Refractive Index
1.5770 - 1.5810 @20?C
Assay (GC)
> 97.5%
Description
2-Hydroxy-5-methoxybenzaldehyde is employed to study electroantennogram response of the vine weevil (Otiorhynchus sulcatus F) to a broad range of volatile plant compounds. It plays an important role in the preparation of tetradentate Schiff base compounds. Further, it is used in the preparation 6-methoxy-3-nitro-2H-chromene by using dibutylamine as a reagent.
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-Hydroxy-5-methoxybenzaldehyde is employed to study electroantennogram response of the vine weevil (Otiorhynchus sulcatus F) to a broad range of volatile plant compounds. It plays an important role in the preparation of tetradentate Schiff base compounds. Further, it is used in the preparation 6-methoxy-3-nitro-2H-chromene by using dibutylamine as a reagent.
Solubility
Miscible with chloroform. Slightly miscible with water.
Notes
Air sensitive. Incompatible with strong oxidizing agents and strong bases.
2-Hydroxy-5-methoxybenzaldehyde is employed to study electroantennogram response of the vine weevil (Otiorhynchus sulcatus F) to a broad range of volatile plant compounds. It plays an important role in the preparation of tetradentate Schiff base compounds. Further, it is used in the preparation 6-methoxy-3-nitro-2H-chromene by using dibutylamine as a reagent.
Solubility
Miscible with chloroform. Slightly miscible with water.
Notes
Air sensitive. Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
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