13160-56-0

Basic information

• Product Name: N-(4-hydroxyphenyl)-4-nitrobenzamide
• Synonyms: benzamide, N-(4-hydroxyphenyl)-4-nitro-; N-(4-Hydroxyphenyl)-4-nitrobenzamide
• CAS NO: 13160-56-0
• Molecular Formula: C₁₃H₁₀N₂O₄
• Molecular Weight: 258.2295
• Mol File: 13160-56-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 395.8°C at 760 mmHg
• Flash Point: 193.2°C
• Density: 1.446g/cm³
• Vapor Pressure: 7.83E-07mmHg at 25°C
• Refractive Index: 1.703
• CAS DataBase Reference: N-(4-hydroxyphenyl)-4-nitrobenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-hydroxyphenyl)-4-nitrobenzamide(13160-56-0)
• EPA Substance Registry System: N-(4-hydroxyphenyl)-4-nitrobenzamide(13160-56-0)

Safety Data

• Hazardous Substances Data: 13160-56-0(Hazardous Substances Data)

Upstream product

• 123-30-8 4-amino-phenol 
• 122-04-3 4-nitro-benzoyl chloride 
• 51-78-5 p-aminophenol hydrochloride 
• 2029-61-0 N-hydroxy-N-phenyl-4-nitrobenzamide 
• 100-65-2 N-Phenylhydroxylamine 
• 98-95-3 nitrobenzene 

Downstream Products

• 102591-20-8 1-(4-nitro-benzoylamino)-4-(3,4,5-trimethoxy-benzoyloxy)-benzene 
• 19208-04-9 2-morpholin-4-ylmethyl-4-(4-nitro-benzoylamino)-phenol 
• 90446-41-6 N-(4-Hydroxy-3,5-bis-pyrrolidin-1-ylmethyl-phenyl)-4-nitro-benzamide 
• 90446-62-1 N-(4-aminobenzoyl)-3,5-bis(pyrrolidinylmethyl)-4-hydroxyaniline 
• 76960-33-3 4-nitro-N-(4-oxocyclohexa-2,5-dien-1-ylidene)benzamide 
• 1489231-09-5 N-(3-((7H-purin-6-yl)thio)-4-hydroxyphenyl)-4-nitrobenzamide 
• 1489235-56-4 N-(3-((1H-1,2,4-triazol-5-yl)thio)-4-hydroxyphenyl)-4-nitrobenzamide 
• 1489235-57-5 N-(4-hydroxy-3-((5-methyl-1,3,4-thiadiazol-2-yl)thio)phenyl)-4-nitrobenzamide 
• 1489231-05-1 N-(3-((1,3,4-thiadiazol-2-yl)thio)-4-hydroxyphenyl)-4-nitrobenzamide 

Relevant articles and documents

Redox-Neutral Selenium-Catalysed Isomerisation of para-Hydroxamic Acids into para-Aminophenols

A selenium-catalysed para-hydroxylation of N-aryl-hydroxamic acids is reported. Mechanistically, the reaction comprises an N?O bond cleavage and consecutive selenium-induced [2,3]-rearrangement to deliver para-hydroxyaniline derivatives. The mechanism is studied through both 18O-crossover experiments as well as quantum chemical calculations. This redox-neutral transformation provides an unconventional synthetic approach to para-aminophenols.

Synthesis and Antiarrhythmic and Parasympatholytic Properties of Substituted Phenols. 2. Amides

Thirty amides patterned after the antiarrhythmic drug changrolin were synthesized and their antiarrhythmic and parasympatholytic activities were assessed. There was no correlation between antiarrhythmic and parasympatholytic activities. Several of the ami