1416547-86-8

Basic information

• Product Name: 4-(phenylselanyl)-2H-benzo[h]chromene
• Synonyms: 4-(phenylselanyl)-2H-benzo[h]chromene
• CAS NO: 1416547-86-8
• Molecular Weight: 337.28
• Mol File: 1416547-86-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(phenylselanyl)-2H-benzo[h]chromene(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(phenylselanyl)-2H-benzo[h]chromene(1416547-86-8)
• EPA Substance Registry System: 4-(phenylselanyl)-2H-benzo[h]chromene(1416547-86-8)

Safety Data

• Hazardous Substances Data: 1416547-86-8(Hazardous Substances Data)

Upstream product

• 34837-55-3 Phenylselenyl bromide 
• 18542-45-5 1-(propargyloxy)naphthalene 
• 1147710-94-8 [3-(naphthalen-1-yloxy)prop-1-ynyl](phenyl)selane 

Relevant articles and documents

Bronsted acid catalyzed intramolecular hydroarylation for the synthesis of cycloalkenyl selenides and tellurides

Trifluoromethanesulfonic acid catalyzed intramolecular hydroarylation of alkynyl selenides and tellurides is developed for the preparation of cycloalkenyl selenide and telluride derivatives through a selective 6- and 7-endo mode. The cycloalkenyl selenides and tellurides can be easily converted into a wide range of other valuable functionalities, including cyclic olefins, allylic alcohols, enynes, 1,3-dienes, and α,β-unsaturated aldehydes. Trifluoromethanesulfonic acid catalyzed intramolecular hydroarylation of alkynyl selenides and tellurides is developed for the preparation of cycloalkenyl selenide and telluride derivatives through a selective 6- and 7-endo mode. The cycloalkenyl selenides and tellurides can be easily converted into a variety of valuable functionalities, including cyclic olefins, allylic alcohols, enynes, 1,3-dienes, and α,β-unsaturated aldehydes. Copyright