1046785-02-7

Basic information

• Product Name: 4-(4-{3,3,4,4,5,5-hexafluoro-2-[2-methyl-5-(4-octyloxyphenyl)thiophen-3-yl]cyclopent-1-enyl}-5-methylthiophen-2-yl)benzoic acid 4-(pyren-1-yl)butyl ester
• Synonyms: 4-(4-{3,3,4,4,5,5-hexafluoro-2-[2-methyl-5-(4-octyloxyphenyl)thiophen-3-yl]cyclopent-1-enyl}-5-methylthiophen-2-yl)benzoic acid 4-(pyren-1-yl)butyl ester
• CAS NO: 1046785-02-7
• Molecular Weight: 949.134
• Mol File: 1046785-02-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(4-{3,3,4,4,5,5-hexafluoro-2-[2-methyl-5-(4-octyloxyphenyl)thiophen-3-yl]cyclopent-1-enyl}-5-methylthiophen-2-yl)benzoic acid 4-(pyren-1-yl)butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-{3,3,4,4,5,5-hexafluoro-2-[2-methyl-5-(4-octyloxyphenyl)thiophen-3-yl]cyclopent-1-enyl}-5-methylthiophen-2-yl)benzoic acid 4-(pyren-1-yl)butyl ester(1046785-02-7)
• EPA Substance Registry System: 4-(4-{3,3,4,4,5,5-hexafluoro-2-[2-methyl-5-(4-octyloxyphenyl)thiophen-3-yl]cyclopent-1-enyl}-5-methylthiophen-2-yl)benzoic acid 4-(pyren-1-yl)butyl ester(1046785-02-7)

Safety Data

• Hazardous Substances Data: 1046785-02-7(Hazardous Substances Data)

Upstream product

• 1046785-00-5 4-(4-{3,3,4,4,5,5-hexafluoro-2-[2-methyl-5-(4-octyloxyphenyl)thiophen-3-yl]cyclopent-1-enyl}-5-methylthiophen-2-yl)benzoic acid 
• 67000-89-9 4-pyrenylbutanol 

Downstream Products

• 1046785-03-8 C₅₆H₅₀F₆O₃S₂ 

Relevant articles and documents

Reversible photoinduced change in molecular ordering of diarylethene derivatives at a solution-HOPG interface

A diarylethene-pyrene diad and a diarylethene-pyrene-diarylethene triad were synthesized to investigate the photoinduced two-dimensional ordering change at a solution-HOPG interface. The molecular arrangements were detected by STM. The different photochromic isomers showed different orderings reflecting the differences in their molecular structures. For the diarylethene-pyrene- diarylethene triad, a new ordering appeared upon irradiation with UV light and returned to the original ordering upon subsequent irradiation with visible light. The new arrangement was assigned to the ordering of the closed-closed isomers based on the images of the isolated open- and closed-isomers. The relationship between the nature of the two-dimensional ordering and the molecular structure is discussed.