75073-52-8

Basic information

• Product Name: Selenophene, 2-(4-methoxyphenyl)-
• CAS NO: 75073-52-8
• Molecular Formula: C11H10OSe
• Molecular Weight: 237.16
• Mol File: 75073-52-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Selenophene, 2-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Selenophene, 2-(4-methoxyphenyl)-(75073-52-8)
• EPA Substance Registry System: Selenophene, 2-(4-methoxyphenyl)-(75073-52-8)

Safety Data

• Hazardous Substances Data: 75073-52-8(Hazardous Substances Data)

Upstream product

• 696-62-8 para-iodoanisole 
• 1449-68-9 2-bromoselenophene 
• 5720-07-0 4-methoxyphenylboronic acid 
• 37686-36-5 2-iodolselenophene 
• 288-05-1 selenophene 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 1963-36-6 4-methoxycinnamaldehyde 
• 1620635-61-1 1-((E)-4,4-dibromobuta-1,3-dienyl)-4-methoxybenzene 
• 24680-50-0 4-methoxy-trans-cinnamaldehyde 

Downstream Products

• 75073-54-0 p-2-selenienylphenol 

Relevant articles and documents

Selenophenol quinoline derivative as well as preparation method and application thereof

The invention discloses a selenophenol quinoline derivative as well as a preparation method and application thereof. The structure of the selenophenol quinoline derivative is shown as a formula I, a formula II or a formula III, wherein R1 is hydrogen, a C1-6 alkyl group, a C1-6 alkoxy group, a substituted ketone group, a phenyl group, a benzyl group, a substituted phenyl group or a substituted benzyl group; R1 is a monovalent metal cation; R2 is one or more of hydrogen, halogen, a C1-4 alkyl group, a C1-4 alkoxy group or a C1-4 haloalkyl group; R3 is a substituted five-membered heterocyclicring or a substituted six-membered heterocyclic ring; and a heteroatom is one or more of N, O, S or Se. The compound disclosed by the invention is novel in structure, simple in preparation process and relatively good in inhibition effect on various cancer cells, particularly the compounds 34, 44, 45, 98, 104, 115 and 116 have excellent inhibition effects on various cancer cells, the effects of the compounds are equivalent to those of a positive control DDP, and the compounds can be used to prepare anti-cancer drugs to be applied under 5 [mu]M or below, so that the prospect is wide.

A direct synthesis of selenophenes by Cu-catalyzed one-pot addition of a selenium moiety to (E,E)-1,3-dienyl bromides and subsequent nucleophilic cyclization

An efficient protocol for the synthesis of selenophenes and selanyl selenophenes has been achieved by a simple one-pot reaction of 1,3-dienyl bromides and 1,3-dienyl-gem-dibromides respectively with KSeCN catalyzed by CuO nanoparticles. Several aryl, alke

Palladium-catalyzed Suzuki cross-coupling of 2-haloselenophenes: Synthesis of 2-arylselenophenes, 2,5-diarylselenophenes, and 2-arylselenophenyl ketones

We present herein our results on the Suzuki coupling reaction of 2-haloselenophenes with boronic acids catalyzed by palladium salt and describe a new route established to prepare 2-arylselenophenes and 2,5-diarylselenophenes in good yields. The reaction p