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

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

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

Relevant articles and documents

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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

Lewis Acid-catalysed Reactions of Aryl Cyclopropyl Ketones. Scope and Mechanism

The effects of aryl substituents on the stannic chloride-catalysed cyclisation of aryl cyclopropyl ketones (1) to aryl tetralones (2) are consistent with the formation of a benzyl carbocation intermediate (8) or a cyclic oxonium ion intermediate (12).The

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

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TRAPPING THE INTERMEDIATE INVOLVED IN THE INTRAMOLECULAR CYCLISATION OF CYCLOPROPYL KETONES. A CONVENIENT PREPARATION OF OPEN-CHAIN γ-HYDROXY KETONES.

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