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Veratraldehyde, 99%
CAS: 120-14-9 | C9H10O3 | 166.18 g/mol
| Catalog Number | Quantity |
|---|---|
| ALFA11110.22 | 100 g |
Catalog number ALFA11110.22
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Quantity:
100 g
Specifications
Chemical Name or MaterialVeratraldehyde
CAS120-14-9
Health Hazard 1H302-H315-H319-H335
Health Hazard 2GHS H Statement
H302-H315-H319-H335
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
H302-H315-H319-H335
Harmful if swallowed.
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
Health Hazard 3P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P501c
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Veratraldehyde was used in the preparation of 4-chloromethyl-2-(dimethoxyphenyl)-1,3-dioxolane. It was used in the synthesis of (+)-lithospermic acid, having anti-HIV activity. It forms 1:1 inclusion complexes with cyclodextrins. It reacts with 3-acetyl-2,5-dimethythiophene to yield chalcone dye, (2E)-3-(3,4-Dimethoxyphenyl)-1-(2,5-dimethylthiophen-3-yl)prop-2-en-1-one.
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
Veratraldehyde was used in the preparation of 4-chloromethyl-2-(dimethoxyphenyl)-1,3-dioxolane. It was used in the synthesis of (+)-lithospermic acid, having anti-HIV activity. It forms 1:1 inclusion complexes with cyclodextrins. It reacts with 3-acetyl-2,5-dimethythiophene to yield chalcone dye, (2E)-3-(3,4-Dimethoxyphenyl)-1-(2,5-dimethylthiophen-3-yl)prop-2-en-1-one.
Solubility
Soluble in water. Freely soluble in alcohol and ether.
Notes
Air sensitive. Incompatible with oxidizing agents.
Veratraldehyde was used in the preparation of 4-chloromethyl-2-(dimethoxyphenyl)-1,3-dioxolane. It was used in the synthesis of (+)-lithospermic acid, having anti-HIV activity. It forms 1:1 inclusion complexes with cyclodextrins. It reacts with 3-acetyl-2,5-dimethythiophene to yield chalcone dye, (2E)-3-(3,4-Dimethoxyphenyl)-1-(2,5-dimethylthiophen-3-yl)prop-2-en-1-one.
Solubility
Soluble in water. Freely soluble in alcohol and ether.
Notes
Air sensitive. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Tirumala G.Varadaraju; Jih Ru Hwu. Synthesis of anti-HIV lithospermic acid by two diverse strategies. Organic & Biomolecular Chemistry. 2012, 10,(28), 5456-5465.
- Abdullah M.Asiri; Hadi M.Marwani; Salman A.Khan; Samy A.El-Daly. Investigation of spectroscopic behaviors of newly synthesized (2E)-3-(3,4-dimethoxyphenyl)-1-(2,5-dimethylthiophen-3-yl)prop-2-en-1-one (DDTP) dye. Journal of Fluorescence. 2013, 23,(6), 1271-1278.
- Can be used to protect diols as their cyclic 3,4-dimethoxybenzylidene acetals: Tetrahedron, 43, 2549 (1987).