950894-31-2

Upstream product

• 1482-82-2 dibenzyl diselenide 
• 886-66-8 1,4-diphenyl-1,3-butadiyne 

Downstream Products

• 950894-38-9 2,5-diphenyl-3-iodoselenophene 
• 1276044-03-1 C₂₃H₁₇BrSe 
• 1276044-04-2 3-benzyl-2,4,5-triphenylselenophene 
• 1276044-05-3 3-benzyl-4-(4-methoxyphenyl)-2,5-diphenylselenophene 
• 1276044-06-4 3-benzyl-2,5-diphenyl-4-p-tolylselenophene 
• 1276044-07-5 1-(4-(4-benzyl-2,5-diphenylselenophen-3-yl)-phenyl)ethanone 
• 1276044-08-6 3-benzyl-4-(4-chlorophenyl)-2,5-diphenylselenophene 
• 1276044-09-7 3-benzyl-4-(3-nitrophenyl)-2,5-diphenylselenophene 
• 69455-93-2 3-benzyl-2,5-diphenylselenophene 
• 13343-79-8 (E)-1,4-Diphenylbut-1-en-3-yne 
• 1353040-02-4 3-chloro-2,5-diphenylselenophene 
• 1353039-98-1 3-bromo-2,5-diphenylselenophene 
• 685570-02-9 (Z)-1-(n-butylseleno)-1,4-diphenyl-but-1-en-3-yne 
• 18782-55-3 2,5-bis-phenylselenophene 

Relevant academic research and scientific papers

Green synthesis of halogenated thiophenes, selenophenes and benzo[b]selenophenes using sodium halides as a source of electrophilic halogens

Herein, we report the first synthesis of chlorinated benzo[b]selenophenes via environmentally friendly electrophilic chlorocyclization reaction using “table salt” as a source of “electrophilic chlorine” and ethanol as a solvent. In addition, the synthesis

Selective base-promoted synthesis of substituted selenophenes by carbocyclization of (Z)-benzylselenoenynes

We herein described the synthesis of several 3-benzyl-2,5-diarylselenophene derivatives in moderate to good yields using (Z)-benzylselenoenynes as starting material in carbocyclization reactions. The reactions were carried out under mild conditions using

Electrophilic cyclization of (Z)-selenoenynes: Synthesis and reactivity of 3-iodoselenophenes

(Chemical Equation Presented) We present here our results of the electrophilic cyclization reaction of (Z)-selenoenynes with different electrophiles such as I2, ICl, PhSeBr, and PhSeCl. The cyclization reaction proceeded cleanly under mild reac