66668-41-5

Basic information

• Product Name: 1-N-ethyl-4-nitrobenzene-1,2-diaMine
• Synonyms: 1-N-ethyl-4-nitrobenzene-1,2-diaMine;N1-ETHYL-4-NITRO-1,2-PHENYLENEDIAMINE;N1-ethyl-4-nitro-1,2-benzenediamine;N1-ethyl-4-nitrobenzene-1,2-diamine
• CAS NO: 66668-41-5
• Molecular Formula: C₈H₁₁N₃O₂
• Molecular Weight: 181.19184
• Mol File: 66668-41-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 372.7°C at 760 mmHg
• Flash Point: 179.2°C
• Appearance: /
• Density: 1.298g/cm³
• Vapor Pressure: 9.44E-06mmHg at 25°C
• Refractive Index: 1.656
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: 1-N-ethyl-4-nitrobenzene-1,2-diaMine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-N-ethyl-4-nitrobenzene-1,2-diaMine(66668-41-5)
• EPA Substance Registry System: 1-N-ethyl-4-nitrobenzene-1,2-diaMine(66668-41-5)

Safety Data

• Hazardous Substances Data: 66668-41-5(Hazardous Substances Data)

Usage

General Description

1-N-ethyl-4-nitrobenzene-1,2-diamine is an organic compound with the chemical formula C8H11N3O2. It is a derivative of 1,2-diaminobenzene, also known as o-phenylenediamine, with an ethyl group and a nitro group substituted on the benzene ring. 1-N-ethyl-4-nitrobenzene-1,2-diaMine is used in the production of dyes, hair colorants, and rubber chemicals. It is also employed as a reagent in organic synthesis for the preparation of various pharmacologically active compounds. 1-N-ethyl-4-nitrobenzene-1,2-diamine is classified as a hazardous chemical and should be handled with care due to its toxicity and potential to cause skin and eye irritation.

InChI:InChI=1/C8H11N3O2/c1-2-10-8-4-3-6(11(12)13)5-7(8)9/h3-5,10H,2,9H2,1H3

Upstream product

• 3846-50-2 2,4-dinitro-N-ethylaniline 
• 97-00-7 1-chloro-2,4-dinitro-benzene 

Downstream Products

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• 237750-78-6 4-[(5-benzenesulphonylamino-1-ethyl-1H-benzimidazol-2-yl)-methyl]-benzonitrile 
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Relevant articles and documents

BICYCLICALLY SUBSTITUTED URACILS AND THE USE THEREOF

The present application relates to novel bicyclically substituted uracil derivatives, to processes for preparation thereof, to the use thereof alone or in combinations for treatment and/or prophylaxis of diseases, and to the use thereof for production of medicaments for treatment and/or prophylaxis of diseases.

Synthesis and magnetic properties of new binuclear Cu(II) complexes with tridentate azomethine ligands

New binuclear copper complexes of tridentate azomethine ligands with various combinations of N, O, and S donor centers were prepared by various procedures, including template synthesis. The magnetochemical data obtained for the range 2-300 K suggest the occurrence of antiferromagnetic coupling in most of these chelates. The only exception is the complex containing N-tosyl and N-ethyl donor fragments, in which the ferromagnetic exchange is observed. Nauka/Interperiodica 2006.

Synthesis of 6-alkyl/aralkyl-5a,11-dihydro-9-nitro[1]benzopyrano[2,3-b][1,5]benzod azepin-13-ones as possible antipsychotic agents

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