1350431-48-9

Basic information

• Product Name: 4-methoxy-2-(methylselenyl)benzaldehyde
• Synonyms: 4-methoxy-2-(methylselenyl)benzaldehyde
• CAS NO: 1350431-48-9
• Molecular Weight: 229.137
• Mol File: 1350431-48-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4-methoxy-2-(methylselenyl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-2-(methylselenyl)benzaldehyde(1350431-48-9)
• EPA Substance Registry System: 4-methoxy-2-(methylselenyl)benzaldehyde(1350431-48-9)

Safety Data

• Hazardous Substances Data: 1350431-48-9(Hazardous Substances Data)

Upstream product

• 7101-31-7 dimethyl diselenide 
• 331-64-6 2-fluoro-4-methoxy-benzaldehyde 

Relevant articles and documents

anti-oxidant composition comprising resveratrol analogues

The present invention provides an antioxidant composition containing a compound represented by chemical formula 1 as an antioxidant active component. In the chemical formula 1, X is O, S, or Se, and each R is independently selected from among hydrogen, an alkyl group having 1 to 12 carbon atoms, and an arylalkyl group having 7 to 15 carbon atoms. The present invention exhibits an excellent antioxidative effect, thereby being useful as the antioxidant composition.COPYRIGHT KIPO 2019

NOVEL METHOD FOR PREPARING SELENYL-SUBSTITUTED AROMATIC ALDEHYDE COMPOUNDS

A, [...] -substituted aromatic aldehydes (selenyl-substituted aromatic aldehyde) compound relates to novel manufacturing method, specifically, form (selenolate nucleophile) nucleophile [...] aromatic aldehyde-based starting material including the nucleoph

Mild generation of selenolate nucleophiles by thiol reduction of diselenides: Convenient syntheses of selenyl-substituted aryl aldehydes

Various selenyl-substituted aryl aldehydes were obtained using dithiothreitol (DTT) as a reducing agent for diselenides in the presence of a base. For electron-deficient haloaryl aldehydes, a weak base, such as K 2CO3, performed well. However, for electron-rich haloaryl aldehydes, a stronger base, such as 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), was required for successful substitution. The selenyl-substitution of heteroaryl substrates were also investigated to obtain satisfactory yields of the desired products.