22692-70-2

Basic information

• Product Name: Benzene, 1,1'-(1-ethyl-1,2-ethenediyl)bis-
• Synonyms: Stilbene, α-ethyl-;1,2-diphenyl-but-1-ene
• CAS NO: 22692-70-2
• Molecular Formula: C16H16
• Molecular Weight: 208.303
• Mol File: 22692-70-2.mol
• Article Data: 9

Chemical Properties

• Melting Point: 57°C
• Boiling Point: 322.51°C (rough estimate)
• Density: 1.0124
• Refractive Index: 1.5930
• CAS DataBase Reference: Benzene, 1,1'-(1-ethyl-1,2-ethenediyl)bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(1-ethyl-1,2-ethenediyl)bis-(22692-70-2)
• EPA Substance Registry System: Benzene, 1,1'-(1-ethyl-1,2-ethenediyl)bis-(22692-70-2)

Safety Data

• Hazardous Substances Data: 22692-70-2(Hazardous Substances Data)

Upstream product

• 93-55-0 1-phenyl-propan-1-one 
• 100-52-7 benzaldehyde 
• 103-65-1 phenylpropane 
• 667458-78-8 benzyl 3,5-bis(trifluoromethyl)phenyl sulfone 
• 100-39-0 benzyl bromide 
• 863560-55-8 [3,5-bis(trifluoromethyl)phenyl] benzyl sulfide 
• 917481-53-9 1-phenylpropyl 3,5-bis(trifluoromethyl)phenyl sulfone 
• 74-96-4 ethyl bromide 
• 98-07-7 Benzotrichlorid 
• 908094-04-2 phenyldiazomethane 
• 52686-70-1 triethylamine-1-(2-naphthylethyl)borane 
• 4426-62-4 1,2-diphenyl-2-butanol 
• 1080-32-6 O,O-diethyl benzylphosphonate 
• 74-85-1 ethene 

Downstream Products

• 100-52-7 benzaldehyde 
• 93-55-0 1-phenyl-propan-1-one 
• 5223-59-6 1,2-diphenylbutane 
• 16939-12-1 2,3-diphenylthiophene 

Relevant articles and documents

ARYL ISONITRILES AS A NEW CLASS OF ANTIMICROBIAL COMPOUNDS

The present invention provides aryl isonitrile compounds that have antibacterial properties. More specifically, the aryl isonitrile compounds of the present invention are potent inhibitors of drug resistant strains of Staphylococcus aureus.

SnCl4-Zn: A novel reductive system for deoxygenative coupling of aliphatic, aromatic, chalcone epoxide, and indanone carbonyl compounds to olefins

SnCl4-Zn complex provided a novel reductive system in the deoxygenative cross-coupling of aliphatic, aromatic, chalcone epoxide and indanone carbonyl compounds to olefins in high yield (55-86%) at reflux temperature in THF. The advantage of this reagent is inexpensive, short reaction time, and high yield compared to the reagents used in the McMurry cross-coupling reaction.

3,5-Bis(trifluoromethyl)phenyl sulfones in the Julia-Kocienski olefination - Application to the synthesis of tri- and tetrasubstituted olefins

3,5-Bis(trifluoromethyl)phenyl (BTFP) sulfones 8a-d are successfully employed in the modified Julia olefination reaction with carbonyl compounds employing phosphazene base P4-tBu at room temp. in THF, affording tri- and tetrasubstituted olefins in good yi