5493-73-2

Basic information

• Product Name: Benzene, 1-(cyclohexyloxy)-4-nitro-
• Synonyms: 1-cyclohexyloxy-4-nitrobenzene;cyclohexyl-(4-nitro-phenyl)-ether;1-cyclohexyloxy-4-nitro-benzene;cyclohexyl 4-nitrophenyl ether;(p-nitrophenoxy)cyclohexane;Cyclohexyl-(4-nitro-phenyl)-aether
• CAS NO: 5493-73-2
• Molecular Formula: C12H15NO3
• Molecular Weight: 221.256
• Mol File: 5493-73-2.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(cyclohexyloxy)-4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(cyclohexyloxy)-4-nitro-(5493-73-2)
• EPA Substance Registry System: Benzene, 1-(cyclohexyloxy)-4-nitro-(5493-73-2)

Safety Data

• Hazardous Substances Data: 5493-73-2(Hazardous Substances Data)

Upstream product

• 108-85-0 1-bromocyclohexane 
• 28341-54-0 4-(4-nitrophenoxy)butanoic acid 
• 100-02-7 4-nitro-phenol 
• 110-83-8 cyclohexene 
• 100-00-5 4-chlorobenzonitrile 
• 108-93-0 cyclohexanol 
• 636-98-6 p-nitrobenzene iodide 
• 824-78-2 4-nitrophenol sodium salt 
• 350-46-9 4-Fluoronitrobenzene 

Downstream Products

• 39905-48-1 4-(cyclohexyloxy)benzenamine 
• 76198-54-4 chloro-acetic acid-(4-cyclohexyloxy-anilide) 
• 85003-35-6 2-Chloro-3-(4-cyclohexyloxy-phenyl)-propionic acid methyl ester 
• 85010-69-1 5-(4-Cyclohexyloxy-benzyl)-2-imino-thiazolidin-4-one 
• 85010-79-3 2-bromo-3-<4-(1-methylcyclohexylmethoxy)phenyl>propionitrile 
• 438590-19-3 dimethyl 6-cyclohexyloxyquinoline-2,4-dicarboxylate 

Relevant articles and documents

AGRICULTURAL CHEMICALS

The present invention relates to picolinic acid derivatives that are useful in treating fungal diseases ofplants.

Fe3O4@mesoporouspolyaniline: A highly efficient and magnetically separable catalyst for cross-coupling of aryl chlorides and phenols

A high surface, magnetic Fe3O4@mesoporouspolyaniline core-shell nanocomposite was synthesized from magnetic iron oxide (Fe 3O4) nanoparticles and mesoporouspolyaniline (mPANI). The novel porous magnetic Fe3O4 was obtained by solvothermal method under sealed pressure reactor at high temperature to achieve high surface area. The mesoporouspolyaniline shell was synthesized by in situ surface polymerization onto porous magnetic Fe3O4 in the presence of polyvinylpyrrolidone (PVP) and sodium dodecylbenzenesulfonate (SDBS), as a linker and structure-directing agent, through 'blackberry nanostructures' assembly. The material composition, stoichiometric ratio and reaction conditions play vital roles in the synthesis of these nanostructures as confirmed by variety of characterization techniques. The role of the mesoporouspolyaniline shell is to stabilize the porous magnetic Fe3O4 nanoparticles, and provide direct access to the core Fe3O4 nanoparticles. The catalytic activity of magnetic Fe3O 4@mesoporousPANI nanocomposite was evaluated in the cross-coupling of aryl chlorides and phenols. Copyright

PIPERIDINE DERIVATIVES AS HUMAN PAPILLOMA VIRUS INHIBITORS

HPV inhibitors with formula (I) where G1 represents a hydrocarbonated bond or chain possibly substituted by one or two alkyl groups, G2 represents a group (see formula Ia+Ib) or R represents a hydrogen, an alkyl, halogenoalkyl, or a prodrug radical such as carbamate, acetyl or dialkylaminomethyl, G represents a bond or a hydrocarbonated chain possibly substituted by one or two alkyls, W represents an oxygen or sulphur, R1 and R2 each represent a group chosen from among hydrogen, halogen, hydroxyl, thio, alkoxy, halogenoalkoxy, alkylthio, halogenoalkylthio, amino, monoalkylamino, dialkylamino, cycloalkyl, alkyl or halogenoalkyl, R3 represents an acid or a prodrug radical of the acid function or a bioisostere of the acid function, A represents an aryl, cycloalkyl, cycloalkenyl or a heterocycle, each possibly substituted, and B represents an aryl or a heterocycle with 6 chains, each possibly substituted, and pharmaceutically acceptable salts.