37686-36-5

Basic information

• Product Name: 2-iodoselenophene
• Synonyms: 2-Iodoselenophene
• CAS NO: 37686-36-5
• Molecular Formula: C₄H₃ISe
• Molecular Weight: 256.9311
• Mol File: 37686-36-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 217.5°C at 760 mmHg
• Flash Point: 85.3°C
• Vapor Pressure: 0.195mmHg at 25°C
• CAS DataBase Reference: 2-iodoselenophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-iodoselenophene(37686-36-5)
• EPA Substance Registry System: 2-iodoselenophene(37686-36-5)

Safety Data

• Hazardous Substances Data: 37686-36-5(Hazardous Substances Data)

Upstream product

• 288-05-1 selenophene 

Downstream Products

• 1123312-64-0 2-(4-ethoxy-2,3-difluorophenyl)selenophene 
• 1123312-60-6 2-[4-(4-propylcyclohexyl)phenyl]selenophene 
• 75073-54-0 p-2-selenienylphenol 
• 1123312-63-9 2-(4-trifluoromethoxyphenyl)selenophene 
• 53390-84-4 2-phenylselenophene 
• 39082-09-2 (phenyl)(selenophen-2-yl)methanone 
• 75073-52-8 2-(4-methoxyphenyl)selenophene 

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.

COMPOUND FOR ORGANIC PHOTOELECTRIC DEVICE AND ORGANIC PHOTOELECTRIC DEVICE, IMAGE SENSOR AND ELECTRONIC DEVICE INCLUDING THE SAME

PROBLEM TO BE SOLVED: To provide a compound for an organic photoelectric device being capable of selectively absorbing light in a green wavelength region, and an organic photoelectric device, an image sensor and an electronic device include the same. SOLUTION: A compound for an organic photoelectric device is represented by Chemical Formula 1, where the definitions of substituents are as described in the specifications. SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2017,JPOandINPIT

Carbon-sulfur bond formation from 2-halochalcogenophenes via copper catalyzed thiol cross-coupling

We present herein our results of the thiol coupling reaction of 2-halochalcogenophenes with Cu(I) and establish the first route to prepare (2-sulfides)-chalcogenophenes in good yields. The reaction performed with both electron donating and electron withdrawing substituents on thiol in the absence of any supplementary additives. In addition, the reaction proceeded cleanly under mild reaction conditions and was sensitive to nature of catalyst, base, and solvent.