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4-ethyl-2-fluoroaniline is a chemical compound with the molecular formula C8H10FN. It is a derivative of aniline, featuring a fluorine atom and an ethyl group attached to the nitrogen atom. 4-ethyl-2-fluoroaniline is known for its role as an intermediate in various chemical syntheses and is recognized for its potential toxicity and irritant properties, necessitating careful handling and use with appropriate safety measures.

821791-69-9

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821791-69-9 Usage

Uses

Used in Pharmaceutical Industry:
4-ethyl-2-fluoroaniline serves as an essential intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Dye Industry:
In the dye industry, 4-ethyl-2-fluoroaniline is utilized for the production of dyes with particular color characteristics. Its chemical structure enables the creation of dyes that can be used in a variety of applications, including textiles, plastics, and printing inks.
Used in Agrochemical Industry:
4-ethyl-2-fluoroaniline plays a role in the agrochemical sector as a precursor for the synthesis of various agrochemicals. Its contribution to the development of pesticides and other agricultural chemicals helps in enhancing crop protection and productivity.
Used in Organic Compounds Manufacturing:
4-ethyl-2-fluoroaniline is also employed in the manufacturing of organic compounds, where its specific properties can be leveraged to create new materials with unique characteristics for a range of applications.
Used in Organic Synthesis as a Precursor:
As a precursor in organic synthesis, 4-ethyl-2-fluoroaniline is crucial for the production of a variety of complex organic molecules. Its presence in the synthesis process can lead to the development of innovative compounds for diverse industries.

Check Digit Verification of cas no

The CAS Registry Mumber 821791-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,1,7,9 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 821791-69:
(8*8)+(7*2)+(6*1)+(5*7)+(4*9)+(3*1)+(2*6)+(1*9)=179
179 % 10 = 9
So 821791-69-9 is a valid CAS Registry Number.

821791-69-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethyl-2-fluoroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-ethyl-2-fluoro

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:821791-69-9 SDS

821791-69-9Relevant academic research and scientific papers

SULFONYL-SUBSTITUTED BICYCLIC COMPOUND WHICH ACTS AS ROR INHIBITOR

-

, (2020/08/16)

Provided is a sulfonyl-substituted bicyclic compound (A) which acts as a RORγ inhibitor, said compound has good RORγ inhibitory activity and is expected to be used for treating diseases mediated by a RORγ receptor in mammals.

Anion ligand promoted selective C-F bond reductive elimination enables C(sp2)-H fluorination

Mao, Yang-Jie,Luo, Gen,Hao, Hong-Yan,Xu, Zhen-Yuan,Lou, Shao-Jie,Xu, Dan-Qian

supporting information, p. 14458 - 14461 (2019/12/09)

A detailed mechanism study on the anion ligand promoted selective C-H bond fluorination is reported. The role of the anion ligand has been clarified by experimental evidence and DFT calculations. Moreover, the nitrate promoted C-F bond reductive elimination enabled a selective C-H bond fluorination of various symmetric and asymmetric azobenzenes to access diverse o-fluoroanilines.

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