28218-20-4

Basic information

• Product Name: 2-Cyclohexen-1-one, 5,5-dimethyl-3-(2-phenylethenyl)-, (E)-
• CAS NO: 28218-20-4
• Molecular Formula: C16H18O
• Molecular Weight: 226.318
• Mol File: 28218-20-4.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 5,5-dimethyl-3-(2-phenylethenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 5,5-dimethyl-3-(2-phenylethenyl)-, (E)-(28218-20-4)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 5,5-dimethyl-3-(2-phenylethenyl)-, (E)-(28218-20-4)

Safety Data

• Hazardous Substances Data: 28218-20-4(Hazardous Substances Data)

Upstream product

• 126-81-8 dimedone 
• 6783-05-7 trans-2-phenylvinylboronic acid 
• 92249-36-0 5,5-dimethyl-3-oxocyclohex-1-en-1-yl 4-nitrobenzenesulfonate 
• 536-74-3 phenylacetylene 
• 6783-04-6 (E)-2-(2'-phenylethenyl)-1,3,2-benzodioxaborole 
• 100-52-7 benzaldehyde 
• 161670-50-4 7-(α-oxybenzyl)isophorone 
• 108162-13-6 Z-styryl n-butyltelluride 
• 78998-88-6 5,5-dimethyl-3-(phenylseleno)-2-cyclohexen-1-one 
• 78-59-1 3,5,5-Trimethylcyclohex-2-en-1-one 
• 17530-69-7 3-chloro-5,5-dimethylcyclohex-2-en-1-one 
• 28557-00-8 phenylzinc chloride 
• 119441-89-3 (E)-(2-bromoethenyl)diisopropoxyborane 

Relevant articles and documents

Tandem aldol condensation-Diels-Alder-aromatization sequence of reactions: A new pathway for the synthesis of 2-tetralone derivatives

A series of new polysubstituted derivatives of 2-tetralones possessing two ester groups were synthesized via a tandem aldol condensation-Diels-Alder-aromatization sequence of reactions. All the three steps took place in one pot and in the presence of amin

Vinyl nosylates: An ideal partner for palladium-catalyzed cross-coupling reactions

In a hurry to leave! Nosylates act as an excellent leaving group in various palladium-catalyzed cross-couplings, such as Suzuki, Stille, Heck, and Sonogashira reactions (see scheme). Crystalline, stable, and cheap vinyl and aryl nosylates proved better th

A novel and efficient tandem aldol condensation-Diels-Alder reaction pathway for the direct synthesis of dehydrodecaline derivatives

An efficient direct synthesis of dehydrodecaline derivatives is reported via a tandem aldol condensation-Diels-Alder cycloaddition process under Lewis acidic conditions. Addition of dienophile moieties to conjugated dienes, formed in situ from the condens