136-79-8 Usage
Uses
Used in Dye and Pigment Industry:
2-Ethoxy-5-nitroaniline is used as a chemical intermediate for the production of dyes and pigments, contributing to the coloration and stability of these products in various applications such as textiles, plastics, and printing inks.
Used in Pharmaceutical Industry:
As an intermediate in the synthesis of pharmaceuticals, 2-Ethoxy-5-nitroaniline plays a crucial role in the development of new drugs and medicinal compounds, potentially leading to advancements in healthcare and treatment options.
Used in Organic Compounds Synthesis:
2-Ethoxy-5-nitroaniline is utilized as a building block in the synthesis of various organic compounds, expanding its applications across different chemical and industrial sectors.
Safety Precautions:
Given its classification as a hazardous substance, it is imperative to handle and store 2-ethoxy-5-nitroaniline with care. Adhering to safety guidelines and protocols is essential to minimize the risk of exposure and potential health hazards, ensuring the well-being of individuals involved in its production, use, and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 136-79-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136-79:
(5*1)+(4*3)+(3*6)+(2*7)+(1*9)=58
58 % 10 = 8
So 136-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O3/c1-2-13-8-4-3-6(10(11)12)5-7(8)9/h3-5H,2,9H2,1H3
136-79-8Relevant academic research and scientific papers
Regioselective Reduction of Substituted Dinitroarenes Using Baker's Yeast
Davey, Claire L.,Powell, Lawson W.,Turner, Nicholas J.,Wells, Andrew
, p. 7867 - 7870 (2007/10/02)
A range of substituted dinitroaromatic compounds have been reduced using baker's yeast (Saccharamyces cerevisiae), in some cases with very high selectivity.A model is presented to account for the origin of the selectivity together with a possible mechanism for the reduction.
PARTIAL REDUCTION OF DINITROARENES TO NITROANILINES WITH HYDRAZINE HYDRATE.
Avyyangar,Kalkote,Lugade,Nikrad,Sharma
, p. 3159 - 3164 (2007/10/02)
Dinitroarenes containing substituents such as hydroxyl and amine groups could be conveniently reduced with 3 molar equivalents of hydrazine hydrate in presence of Raney nickel catalyst in ethanol/1,2-dichloro-ethane solvent mixture to give a product wherein one of the two nitro groups was reduced to the amino group. The yields of the partial reduction products are good. Under similar conditions alkoxyl substitutes in the o,p-position to the nitro groups were displaced by the hydrazine to give 2,4-dinitrophenyl-hydrazine as the main product. The details of the reduction reaction are described.
