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Atomfair Benzaldehyde, 4-(ethylthio)-2,5-dimethoxy- C11H14O3S
Description Benzaldehyde, 4-(ethylthio)-2,5-dimethoxy- (CAS No. 132184-34-0) is a high-purity organic compound with the molecular formula C11H14O3S. This specialized benzaldehyde derivative features an ethylthio substituent at the 4-position and methoxy groups at the 2- and 5-positions, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. With an IUPAC name of 4-ethylsulfanyl-2,5-dimethoxybenzaldehyde , this compound is characterized by its distinct aromatic aldehyde functionality, which is highly reactive in condensation and nucleophilic addition reactions. Suitable for researchers and scientists, our product is rigorously tested for purity and consistency, ensuring optimal performance in advanced chemical synthesis. Available in various quantities to…
Description
Description
Benzaldehyde, 4-(ethylthio)-2,5-dimethoxy- (CAS No. 132184-34-0) is a high-purity organic compound with the molecular formula C11H14O3S. This specialized benzaldehyde derivative features an ethylthio substituent at the 4-position and methoxy groups at the 2- and 5-positions, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. With an IUPAC name of 4-ethylsulfanyl-2,5-dimethoxybenzaldehyde, this compound is characterized by its distinct aromatic aldehyde functionality, which is highly reactive in condensation and nucleophilic addition reactions. Suitable for researchers and scientists, our product is rigorously tested for purity and consistency, ensuring optimal performance in advanced chemical synthesis. Available in various quantities to meet laboratory-scale and industrial needs.
- CAS No: 132184-34-0
- Molecular Formula: C11H14O3S
- Molecular Weight: 226.29
- Exact Mass: 226.06636548
- Monoisotopic Mass: 226.06636548
- IUPAC Name: 4-ethylsulfanyl-2,5-dimethoxybenzaldehyde
- SMILES: CCSC1=C(C=C(C(=C1)OC)C=O)OC
- Synonyms: 132184-34-0, Benzaldehyde, 4-(ethylthio)-2,5-dimethoxy-, 4-(ETHYLSULFANYL)-2,5-DIMETHOXYBENZALDEHYDE, 4-(Ethylthio)-2,5-dimethoxybenzaldehyde, NLFKCRKWYGOBKL-UHFFFAOYSA-N
Application
Benzaldehyde, 4-(ethylthio)-2,5-dimethoxy-, serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its reactive aldehyde group enables participation in Schiff base formation, Grignard reactions, and other carbonyl-based transformations. The compound’s unique substitution pattern makes it valuable for designing novel heterocyclic compounds and functional materials. Researchers also utilize it in the development of specialty chemicals with potential biological activity.
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