35729-40-9

Basic information

• Product Name: Benzaldehyde, 4-(methylseleno)-
• Synonyms: 4-Methylselanyl-benzaldehyd;4-methylselanyl-benzaldehyde
• CAS NO: 35729-40-9
• Molecular Formula: C8H8OSe
• Molecular Weight: 199.111
• Mol File: 35729-40-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 100 °C(Press: 0.5 Torr)
• Density: 1.5427 g/cm3
• CAS DataBase Reference: Benzaldehyde, 4-(methylseleno)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 4-(methylseleno)-(35729-40-9)
• EPA Substance Registry System: Benzaldehyde, 4-(methylseleno)-(35729-40-9)

Safety Data

• Hazardous Substances Data: 35729-40-9(Hazardous Substances Data)

Upstream product

• 17100-68-4 2-((4-bromobenzyl)oxy)tetrahydro-2H-pyran 
• 195388-59-1 2-(4-Methylselanyl-benzyloxy)-tetrahydro-pyran 
• 7101-31-7 dimethyl diselenide 
• 100-52-7 benzaldehyde 
• 106-40-1 4-bromo-aniline 
• 32449-46-0 1-bromo-4-selenocyanatobenzene 
• 40400-25-7 (4-bromophenyl)(methyl)selane 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 1356922-81-0 (E)-4-(methylseleno)benzaldehyde oxime 
• 1356922-80-9 4-methylselenobenzylamine 
• 1356922-71-8 2-methylthio-4-(4'-methylselenobenzyl)aminoquinazoline 

Relevant articles and documents

Bifunctional chiral selenium-containing 1,4-diarylazetidin-2-ones with potent antitumor activities by disrupting tubulin polymerization and inducing reactive oxygen species production

Organoselenium compounds have attracted growing interests as promising antitumor agents over recent years. Herein, four series of novel selenium-containing chiral 1,4-diarylazetidin-2-ones were asymmetrically synthesized and biologically evaluated for ant

Porphyrin architectures constructed by CH...π interactions: Synthesis and crystal structures of 5,10,15,20-tetrakis(4-methylchalcogenophenyl)-21H,23H-porphyrins

Tetraphenylporphyrins substituted with methylchalcogeno groups (XMe: X = Te, Se, S, and O) were prepared. Crystal structure analysis revealed that a novel type of molecular alignments was achieved by intermolecular CH...π interactions between XCH3 and porphyrin π-systems.