1428541-15-4

Basic information

• Product Name: (E)-styryl(o-tolyl)-λ³-iodanyl trifluoromethanesulfonate
• Synonyms: (E)-styryl(o-tolyl)-λ³-iodanyl trifluoromethanesulfonate
• CAS NO: 1428541-15-4
• Molecular Weight: 470.251
• Mol File: 1428541-15-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-styryl(o-tolyl)-λ³-iodanyl trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-styryl(o-tolyl)-λ³-iodanyl trifluoromethanesulfonate(1428541-15-4)
• EPA Substance Registry System: (E)-styryl(o-tolyl)-λ³-iodanyl trifluoromethanesulfonate(1428541-15-4)

Safety Data

• Hazardous Substances Data: 1428541-15-4(Hazardous Substances Data)

Upstream product

• 615-37-2 ortho-methylphenyl iodide 
• 1493-13-6 trifluorormethanesulfonic acid 
• 31599-59-4 2-(diacetoxyiodo)toluene 
• 6783-05-7 trans-2-phenylvinylboronic acid 

Downstream Products

• 1428540-96-8 (1E,3Z)-1-phenylocta-1,3-dien-4-yl trifluoromethanesulfonate 
• 1428540-97-9 (Z)-2-((E)-styryl)hex-1-en-1-yl trifluoromethanesulfonate 
• 1428541-01-8 (1Z,3E)-1-cyclopentyl-4-phenylbuta-1,3-dien-1-yl trifluoromethanesulfonate 
• 1428541-02-9 (1Z,3E)-2-cyclopentyl-4-phenylbuta-1,3-dien-1-yl trifluoromethanesulfonate 
• 1428541-03-0 (1Z,3E)-4-phenylbuta-1,3-dien-1-yl trifluoromethanesulfonate 
• 1428540-91-3 (1E,3Z)-4-hexyl-1,6-diphenyl-1,3,5-hexatrien-2-yl trifluoromethanesulfonate 
• 615-37-2 ortho-methylphenyl iodide 
• 140706-26-9 (E)-2-phenylethen-1-yl trifluoromethanesulfonate 
• 1428541-00-7 (2E,4E)-5-phenylpenta-2,4-dien-2-yl trifluoromethanesulfonate 
• 1428540-99-1 (2Z,4E)-5-phenylpenta-2,4-dien-2-yl trifluoromethanesulfonate 
• 1428540-71-9 (3Z,5E)-4-ethyl-6-phenylhexa-3,5-dien-3-yl trifluoromethanesulfonate 
• 1428540-72-0 (3E,5E)-4-ethyl-6-phenylhexa-3,5-dien-3-yl trifluoromethanesulfonate 
• 1428541-09-6 N-((3Z,5E)-4-ethyl-6-phenylhexa-3,5-dien-3-yl)benzamide 
• 1428540-73-1 (2Z,4E)-3-methyl-5-phenylpenta-2,4-dien-2-yl trifluoromethanesulfonate 

Relevant articles and documents

Copper-Catalyzed [2+2+2] Modular Synthesis of Multisubstituted Pyridines: Alkenylation of Nitriles with Vinyliodonium Salts

A [2+2+2] modular synthesis of multisubstituted pyridines, with excellent regioselectivity, has been realized by copper catalysisand involves three distinct components: vinyliodonium salts, nitriles, and alkynes. The reactions proceeded with the facile formation of an aza-butadienylium intermediate by alkenylation of the nitrile with a vinyliodonium salt. Moreover, the alkynes in the reaction were extended to alkenes, which are an advantage of expense and relative scarceness of alkynes.