179803-80-6

Basic information

• Product Name: 9-(4-methoxyphenyl)-10-(4-hydroxyphenyl)anthracene
• Synonyms: 9-(4-methoxyphenyl)-10-(4-hydroxyphenyl)anthracene
• CAS NO: 179803-80-6
• Molecular Weight: 376.455
• Mol File: 179803-80-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 9-(4-methoxyphenyl)-10-(4-hydroxyphenyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(4-methoxyphenyl)-10-(4-hydroxyphenyl)anthracene(179803-80-6)
• EPA Substance Registry System: 9-(4-methoxyphenyl)-10-(4-hydroxyphenyl)anthracene(179803-80-6)

Safety Data

• Hazardous Substances Data: 179803-80-6(Hazardous Substances Data)

Upstream product

• 24672-76-2 9,10-bis-(4-methoxy-phenyl)-anthracene 
• 5720-07-0 4-methoxyphenylboronic acid 
• 158902-11-5 9-Bromo-10-(4-methoxylphenyl)anthracene 
• 523-27-3 9,10-Dibromoanthracene 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 179803-85-1 9-[4-(2-ferrocenylethoxy)phenyl]-10-(4-methoxyphenyl)anthracene 
• 179803-88-4 9-[4-(1-ferrocenoylmethoxy)phenyl]-10-(4-methoxyphenyl)anthracene 
• 179803-87-3 9-[4-(5-ferrocenylpentoxy)phenyl]-10-(4-methoxyphenyl)anthracene 
• 179803-86-2 9-[4-(4-ferrocenylbutoxy)phenyl]-10-(4-methoxyphenyl)anthracene 

Relevant articles and documents

Water-soluble fluorescent polymers that respond to singlet oxygen

Although acenes with more than three fused rings can both fluoresce efficiently and react with singlet oxygen (1O2) rapidly, their hydrophobic nature presents a challenge to their use in aqueous environments. Herein we report a series of fluorescent, water-soluble random copolymers that each comprise (oligoethylene glycol) methacrylate (OEGMA) and one of several diarylacene methacrylates, including a tetracene methacrylate and a tetraceneothiophene methacrylate. Exposure to 1O2 in water oxidizes the pendant acenes, resulting in diminution of their fluorescence intensities. The observed rate of oxidation of the tetracene-containing polymers compares favorably with a commercial 1O2-sensitive dye. Polymers that also include energy-donating coumarin side chains show ratiometric fluorescence changes in response to 1O2.