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Benzenamine, 2-ethyl-4-nitro-, also known as 2-ethyl-4-nitroaniline or 4-nitro-o-ethylaniline, is an organic compound with the chemical formula C8H10N2O2. It is a derivative of aniline, where a nitro group is attached to the 4-position and an ethyl group is attached to the 2-position of the benzene ring. This yellow crystalline solid is used as an intermediate in the synthesis of dyes, pharmaceuticals, and other organic compounds. It is also known for its potential applications in the production of azo pigments and rubber chemicals. Due to its reactivity and the presence of functional groups, it is important to handle this chemical with care, as it may pose health and environmental risks.

6853-29-8

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6853-29-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6853-29-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,5 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6853-29:
(6*6)+(5*8)+(4*5)+(3*3)+(2*2)+(1*9)=118
118 % 10 = 8
So 6853-29-8 is a valid CAS Registry Number.

6853-29-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-4-nitroaniline

1.2 Other means of identification

Product number -
Other names 4-amino-3-ethyl-1-nitrobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6853-29-8 SDS

6853-29-8Relevant academic research and scientific papers

Tailor-made synthesis of N,N,2,6-tetrasubstituted 4-nitroanilines by three-component ring transformation of dinitropyridone

Le, Song Thi,Asahara, Haruyasu,Nishiwaki, Nagatoshi

supporting information, p. 1203 - 1206 (2015/03/04)

The ring transformation of dinitropyridone afforded various kinds of 2,6-disubstituted-4-nitroanilines upon treatment with aliphatic ketones in the presence of ammonium acetate as a nitrogen source, wherein dinitropyridone behaved as the synthetic equival

THIENOPYRIMIDINE COMPOUNDS

-

Page/Page column 0169, (2013/07/19)

The present invention relates to the use of novel compounds of Formula I: wherein all variable substituents are defined as described herein, which are SYK inhibitors and are useful for the treatment of auto-immune and inflammatory diseases.

Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents

-

Page column 138-139, 141, 151, (2010/02/05)

This invention relates to 2-arylimino heterocycles, including 2-arylimino-1,3-thiazolidines, 2-arylimino-2,3,4,5-tetrahydro-1,3-thiazines, 2-arylimino-1,3-thiazolidin-4-ones, 2-arylimino-1,3-thiazolidin-5-ones, and 2-arylimino-1,3-oxazolidines, and their use in modulating progesterone receptor mediated processes, and pharmaceutical compositions for use in such therapies.

Ammonium nickel sulphate mediated nitration of aromatic compounds with nitric acid

Tasneem,Ali,Rajanna,Saiparakash

, p. 1123 - 1127 (2007/10/03)

Aromatic compounds were efficiently nitrated under mild conditions employing ammonium nickel sulphate and nitric acid as a reagent. This procedure works efficiently at room temperature yielding mononitro derivative in fair to good yield with high regioselectivity.

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