174023-08-6

Basic information

• Product Name: (E)-4-((4-methoxyphenyl)diazenyl)benzoic acid
• Synonyms: (E)-4-((4-methoxyphenyl)diazenyl)benzoic acid
• CAS NO: 174023-08-6
• Molecular Weight: 256.261
• Mol File: 174023-08-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-4-((4-methoxyphenyl)diazenyl)benzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4-((4-methoxyphenyl)diazenyl)benzoic acid(174023-08-6)
• EPA Substance Registry System: (E)-4-((4-methoxyphenyl)diazenyl)benzoic acid(174023-08-6)

Safety Data

• Hazardous Substances Data: 174023-08-6(Hazardous Substances Data)

Upstream product

• 105299-45-4 4-(4-hydroxyphenylazo)benzoic acid 
• 74-88-4 methyl iodide 
• 77-78-1 dimethyl sulfate 
• 150-13-0 4-amino-benzoic acid 
• 619-68-1 4-nitrosobenzoic acid 
• 104-94-9 4-methoxy-aniline 

Downstream Products

• 139879-15-5 cholest-6-en-3-yl 4-[(E)-(4-methoxyphenyl)diazenyl]benzoate 
• 237764-54-4 2,4-dinitrophenyl 4-(4'-methoxyphenyl)azobenzoate 
• 225531-75-9 (E)-(4-((4-methoxyphenyl)diazenyl)phenyl)methanol 
• 107321-41-5 (E)-4-((4-methoxyphenyl)diazenyl)benzaldehyde 

Relevant articles and documents

A Redox Isomerization Strategy for Accessing Modular Azobenzene Photoswitches with near Quantitative Bidirectional Photoconversion

Photoswitches capable of accessing two geometric states are highly desirable, especially if their design is modular and incorporates a pharmacophore tethering site. We describe a redox isomerization strategy for synthesizing p-formylazobenzenes from p-nit

Azobenzene-porphyrins

A series of covalently-connected azobenzene-porphyrin derivatives have been synthesised and their photochemical properties investigated. The photochemistry of the porphyrin components is essentially unaltered, but photochemical isomerisation of the azobenzene components can not be detected.