19871-39-7

Basic information

• Product Name: 2-methoxy-N-methyl-5-nitroaniline
• Synonyms: 2-Methoxy-N-methyl-5-nitroaniline; benzenamine, 2-methoxy-N-methyl-5-nitro-
• CAS NO: 19871-39-7
• Molecular Formula: C₈H₁₀N₂O₃
• Molecular Weight: 182.1766
• Mol File: 19871-39-7.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 309.8°C at 760 mmHg
• Flash Point: 141.1°C
• Density: 1.258g/cm³
• Vapor Pressure: 0.000626mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: 2-methoxy-N-methyl-5-nitroaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-N-methyl-5-nitroaniline(19871-39-7)
• EPA Substance Registry System: 2-methoxy-N-methyl-5-nitroaniline(19871-39-7)

Safety Data

• Hazardous Substances Data: 19871-39-7(Hazardous Substances Data)

Upstream product

• 709-09-1 3,4-dimethoxynitrobenzene 
• 74-89-5 methylamine 
• 455-93-6 2-fluoro-1-methoxy-4-nitrobenzene 
• 100-17-4 para-methoxynitrobenzene 
• 99-59-2 3-amino-4-methoxynitrobenzene 
• 137090-11-0 acetic acid-(N-methyl-o-anisidide) 
• 10541-78-3 2-methoxy-N-methylaniline 
• 636-93-1 5-nitroguaiacol 
• 100200-99-5 potassium 2-methoxy-4-nitrophenolate monohydrate 
• 36160-54-0 2-isopropyloxy-1-methoxy-4-nitrobenzene 
• 36160-52-8 2-ethoxy-4-nitroanisole 
• 593-51-1 methylamine hydrochloride 
• 107968-00-3 estrone 4-(2-methoxy-4-nitrophenoxy)butyl ether 
• 82040-91-3 α-Bromo-ω-(2-methoxy-4-nitrophenoxy)butane 

Relevant articles and documents

Assignment of Quaternary Carbons via Two-Bond Heteronuclear Selective NOE Difference, a Useful Structure Elucidation Aid

Very low power irradiation of suitable narrow peaks in the proton frequency range generated NOE enhancement in neighbouring quaternary carbons, positioned two bonds from the irradiated protons.Subsequent FID acquisition under normal broad band decoupling

Arylsulfonanilide ureas

The invention provides compounds, compositions and methods relating to novel arylsulfonanilide derivatives and their use as pharmacologically active agents. The compositions find particular use as pharmacological agents in the treatment of disease states,

Synthesis and Structure of 4,10-Diaza-5'-nitro-2,3-dibenzo-12-crown-4

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