1394313-11-1

Basic information

• Product Name: 4-(2,2-diphenylvinyl)chroman
• Synonyms: 4-(2,2-diphenylvinyl)chroman
• CAS NO: 1394313-11-1
• Molecular Weight: 312.411
• Mol File: 1394313-11-1.mol

Chemical Properties

• CAS DataBase Reference: 4-(2,2-diphenylvinyl)chroman(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2,2-diphenylvinyl)chroman(1394313-11-1)
• EPA Substance Registry System: 4-(2,2-diphenylvinyl)chroman(1394313-11-1)

Safety Data

• Hazardous Substances Data: 1394313-11-1(Hazardous Substances Data)

Upstream product

• 1394312-87-8 5-phenoxy-1,1-diphenylpent-2-yn-1-ol 
• 876317-59-8 (4,4-dibromobut-3-enyloxy)benzene 
• 1394312-96-9 (E)-5-phenoxy-1,1-diphenylpent-2-en-1-ol 
• 22409-86-5 3-phenoxypropionaldehyde 

Relevant articles and documents

Synthesis of Substituted Benzoxacycles via a Pd(II)-Catalyzed Intramolecular Arylation Reaction of Allylic Alcohols

Herein a Pd-catalyzed intramolecular allylation reaction of unprotected allylic alcohols was developed, and the reaction proceeded through a Pd(II)-mediated allylic carbocation species formation, followed by a Friedel-Crafts type annulation to afford functionalized chromanes.

Boronic acid catalysis as a mild and versatile strategy for direct carbo- and heterocyclizations of free allylic alcohols

BAC to the future: Boronic acid catalysis (BAC) was applied to the direct activation of alcohols leading to the preparation of carbocycles (see scheme), benzofurans, tetrahydrofurans, pyrrolidines, pyrans, piperidines, and various polycyclic compounds. The reactions proceed under mild conditions that circumvent the use of reactive leaving groups like halides. Copyright