74305-51-4

Basic information

• Product Name: (1Z)-N-hydroxy-1-[4-(2-methylpropyl)phenyl]ethanimine
• CAS NO: 74305-51-4
• Molecular Formula: C₁₂H₁₇NO
• Molecular Weight: 191.2695
• Mol File: 74305-51-4.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 298.962°C at 760 mmHg
• Flash Point: 179.385°C
• Density: 0.973g/cm³
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.508
• CAS DataBase Reference: (1Z)-N-hydroxy-1-[4-(2-methylpropyl)phenyl]ethanimine(CAS DataBase Reference)
• NIST Chemistry Reference: (1Z)-N-hydroxy-1-[4-(2-methylpropyl)phenyl]ethanimine(74305-51-4)
• EPA Substance Registry System: (1Z)-N-hydroxy-1-[4-(2-methylpropyl)phenyl]ethanimine(74305-51-4)

Safety Data

• Hazardous Substances Data: 74305-51-4(Hazardous Substances Data)

Upstream product

• 38861-78-8 1-(4-isobutyl-phenyl)-ethanone 
• 53648-05-8 ibuproxam 

Downstream Products

• 20331-32-2 N-<4-(2-methylpropyl)phenyl>acetamide 
• 38861-78-8 1-(4-isobutyl-phenyl)-ethanone 
• 111525-01-0 1-(4-(2'-methylpropyl)phenyl)ethyl hydroxylamine 
• 111525-05-4 N-Acetoxy-N-[1-(4-isobutyl-phenyl)-ethyl]-acetamide 
• 164579-51-5 4-(2-methylpropyl)phenylethylamine 
• 1462328-04-6 1-(4-isobutylphenyl)ethan-1-one O-acetyl oxime 
• 1462327-93-0 dimethyl 5-(4-isobutylphenyl)-1H-pyrrole-2,3-dicarboxylate 

Relevant articles and documents

Copper(0)/PPh3-Mediated Bisheteroannulations of o-Nitroalkynes with Methylketoximes Accessing Pyrazo-Fused Pseudoindoxyls

A copper(0)/PPh3-mediated cascade bisheteroannulation reaction of o-nitroalkynes with methylketoximes has been developed that provides viable access to a diverse range of pyrazo-fused pseudoindoxyl compounds. Synthetically useful functional groups including sensitive C-I bonds are compatible with this system. Mechanistic studies suggest a reaction cascade involving sequential PPh3-mediated deoxygenative cycloisomerization and copper-catalyzed [3 + 2] pyrazo-annulation.

Elemental tellurium mediated synthesis of 2-(trifluoromethyl)oxazoles using trifluoroacetic anhydride as reagent

An elemental tellurium mediated synthesis of 2-(trifluoromethyl)oxazoles from the reaction of acetophenone oxime acetates with trifluoroacetic anhydride has been developed. This new tandem cyclization proceeds in good to excellent yields via a SET reduction followed by a 5-endo-trig pathway. Some of the title compounds showed fungicidal and insecticidal activities.

APPLICATIONS OF N6-SUBSTITUTED ADENOSINE DERIVATIVE AND N6-SUBSTITUTED ADENINE DERIVATIVE TO CALMING, HYPNOSES, CONVULSION RESISTANCE, EPILEPTIC RESISTANCE, PARKINSON DISEASE RESISTANCE, AND DEMENTIA PREVENTION AND TREATMENT

PROBLEM TO BE SOLVED: To prepare analgesics, hypnotic agents, anticonvulsant agents, antiepileptics, antiparkinson drugs, dementia prophylactics, and health care food. SOLUTION: The present invention relates to an N6-substituted adenosine derivative and an N6-substituted adenine derivative selected from the group consisting of specific compounds. The present invention also relates to a pharmaceutical composition at least comprising a therapeutically effective amount of the compounds and a pharmaceutically acceptable carrier. The invention further relates to the compounds used in preparation of analgesics, hypnotic agents, anticonvulsant agents, antiepileptics, antiparkinson drugs, dementia prophylactics, and health care food. COPYRIGHT: (C)2016,JPO&INPIT