87815-75-6

Basic information

• Product Name: 4-chloro-N-cyclohexyl-2-nitroaniline
• Synonyms: 4-chloro-N-cyclohexyl-2-nitroaniline
• CAS NO: 87815-75-6
• Molecular Weight: 254.716
• Mol File: 87815-75-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-chloro-N-cyclohexyl-2-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-N-cyclohexyl-2-nitroaniline(87815-75-6)
• EPA Substance Registry System: 4-chloro-N-cyclohexyl-2-nitroaniline(87815-75-6)

Safety Data

• Hazardous Substances Data: 87815-75-6(Hazardous Substances Data)

Upstream product

• 108-91-8 cyclohexylamine 
• 89-61-2 2,5-dichloronitrobenzene 

Downstream Products

• 169117-49-1 7-acetamido-1-cyclohexyl-2,3(1H,4H)-quinoxalinedione 
• 169117-48-0 7-amino-1-cyclohexyl-2,3(1H,4H)-quinoxalinedione 
• 169117-71-9 2-amino-4-chloro-N-cyclohexylaniline 
• 169117-46-8 6-Chloro-1-cyclohexyl-7-nitro-2,3(1H,4H)-quinoxalinedione 
• 169117-47-9 7-amino-6-chloro-1-cyclohexyl-2,3(1H,4H)-quinoxalinedione 
• 169117-45-7 6-Chloro-1-cyclohexyl-2,3(1H,4H)-quinoxalinedione 

Relevant articles and documents

Synthesis of o-Nitroarylamines via Ipso Nucleophilic Substitution of Sulfonic Acids

A mild, efficient, and eco-friendly method for the synthesis of o-nitroarylamine from o-nitroaryl sulfonic acid via ipso nucleophilic aryl substitution by amine is described. The products have been obtained with good yields at room temperature without the assistance of any metal, activating agent, or toxic oxidant. This method is useful for racemization-free synthesis of N-aryl amino acid esters.

Quinoxalines and drugs prepared therefrom

Quinoxaline-2,3-(1H,4H)-diones of the formula I STR1 and their tautomeric and enantiomeric forms and their physiologically tolerated salts, the variables R, R 1 and R 2 have the meanings specified in claim 1, and are useful for therapeutic treatment of neurodegenerative disorders, neurotoxic disturbances or as antiepileptics, antidepressants and anxiolytics; and drugs composed thereof.