78399-02-7

Basic information

• Product Name: N-(3-Nitrothien-2-yl)-N-phenylamine
• Synonyms: N-(3-Nitrothien-2-yl)-N-phenylamine
• CAS NO: 78399-02-7
• Molecular Formula: C10H8N2O2S
• Molecular Weight: 220.252
• Mol File: 78399-02-7.mol

Chemical Properties

• Boiling Point: 375.7±27.0 °C(Predicted)
• Density: 1.404±0.06 g/cm3(Predicted)
• CAS DataBase Reference: N-(3-Nitrothien-2-yl)-N-phenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-Nitrothien-2-yl)-N-phenylamine(78399-02-7)
• EPA Substance Registry System: N-(3-Nitrothien-2-yl)-N-phenylamine(78399-02-7)

Safety Data

• Hazardous Substances Data: 78399-02-7(Hazardous Substances Data)

Upstream product

• 5330-98-3 2-chloro-3-nitrothiophene 
• 62-53-3 aniline 
• 2161-96-8 2-bromo-3-nitrothiophene 
• 159334-00-6 3-nitro-2-phenoxy-thiophene 
• 40018-26-6 1,4-dithiane-2,5-diol 
• 13624-01-6 N-[1-(methylthio)-2-nitroethenyl]benzenamine 
• 33786-81-1 3-nitro-2-(4-nitro-phenoxy)-thiophene 

Relevant articles and documents

An efficient synthesis of N-substituted 3-nitrothiophen-2-amines

A novel protocol for the synthesis of 3-nitro-N-aryl/alkylthiophen-2-amines in good yields from the reaction of α-nitroketene N,S-aryl/alkylaminoacetals and 1,4-dithiane-2,5-diol in the presence of K2CO3 in refluxing ethanol is descr

Aromatic Nucleophilic Substitution Reactions of Some 3-Nitro-2-p-nitrophenoxy-5-X-thiophenes with Substituted Anilines in Methanol

The kinetic constants for the reaction of some 3-nitro-2-p-nitrophenoxy-5-X-thiophenes (X = H, Br, CONH2, CO2Me, Ac, SO2Me, CN,NO2) with some substituted anilines YC6H4NH2 (Y = p-OMe, p-Me, H, n-Cl, p-Cl) have been measured at various temperatures and a s

Aromatic Nucleophilic Substitution Reactions of Some 2-L-3-Nitro-5-X-thiophenes with Piperidine and Aniline in Methanol. Substituent Constants for the Thiophene System

The rate constants for the reactions of some 2-L-3-nitro-5-X-thiophenes 1-4 with aniline and of compounds (4) with piperidine in methanol have been measured at various temperatures.By using the data obtained in this work as well as previously available data sets, a series of optimized 'thiophene' ?τ values has been calculated.The susceptibility constants ρ(L) of the various sets have been analysed in the framework of the reactivity-selectivity principle.

Linear Free Energy Relationships in the Thiophen Series. Part 2. The Kinetics of the Reactions of Some 2-Bromo-3-nitro-5-X-thiophens with Substituted Anilines in Methanol

The rate constants for the reactions of 2-bromo-3-nitro-5-X-thiophens (X=H, Br, CONH2, CO2Me, Ac, SO2Me, CN, or NO2) with some substituted anilines YC6H4NH2 (Y=p-OMe, p-Me, H, m-Cl, or p-CO2Me) have been measured in methanol at various temperatures.The se