6256-06-0

Basic information

• Product Name: 3-bromo-N-(4-chloro-3-nitrophenyl)-4-ethoxybenzamide
• CAS NO: 6256-06-0
• Molecular Formula: C₂₀H₂₂O₅
• Molecular Weight: 399.6238
• Mol File: 6256-06-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 444.3°C at 760 mmHg
• Flash Point: 222.5°C
• Density: 1.606g/cm³
• Vapor Pressure: 4.34E-08mmHg at 25°C
• Refractive Index: 1.654
• CAS DataBase Reference: 3-bromo-N-(4-chloro-3-nitrophenyl)-4-ethoxybenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-N-(4-chloro-3-nitrophenyl)-4-ethoxybenzamide(6256-06-0)
• EPA Substance Registry System: 3-bromo-N-(4-chloro-3-nitrophenyl)-4-ethoxybenzamide(6256-06-0)

Safety Data

• Hazardous Substances Data: 6256-06-0(Hazardous Substances Data)

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 10138-10-0 ethyl 4-oxobutanoate 
• 76934-55-9 (3,4-Dimethoxy-phenyl)-[2-(3,4-dimethoxy-phenyl)-cyclopropyl]-methanone 
• 76934-55-9 (3,4-Dimethoxy-phenyl)-[(1S,2S)-2-(3,4-dimethoxy-phenyl)-cyclopropyl]-methanone 
• 67-56-1 methanol 
• 6380-23-0 3,4-dimethoxystyrene 
• 64-17-5 ethanol 
• 7355-34-2 1,3‐bis(3,4‐dimethoxyphenyl)prop‐2‐en‐1‐one 

Relevant articles and documents

Cerium(IV) ammonium nitrate induced dimerization of methoxystyrenes

4-Methoxystyrene 1 underwent dimerization to 1,4-diphenylbutane derivatives 5 and 6 in presence of CAN in methanol. But in ethanol the same reaction afforded a tetralone derivative along with 5 and 6.3,4- Dimethoxystyrene 10 underwent dimerization in pres

Reactions of Aryl Cyclopropyl Ketones. A New Synthesis of Aryl Tetralones

Aryl cyclopropyl ketones (2) cyclise to 1-tetralones (3) in the presence of a variety of acid catalysts under mild conditions.Open-chain carbinols (4) are also formed.The ratio of (3) to (4) is dependent on the aryl ring substituents.A cationic mechanism is proposed.Cyclopropyl ketones (1) do not react.Stereoelectronic factors involved in the reactivity of the rigig cyclopropyl ketone (12) are discussed.The reactions of selected phenolic cyclopropyl ketones have been investigated as anionic counterparts to the acid-catalysed reactions.No reaction is observed.

Further experimental data on racemic galbuline and its structurally allied compounds

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