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1-Ethoxy-2-methoxy-4-nitrobenzene is an organic compound characterized by the presence of an ethoxy group (-OCH2CH3) at the 1st carbon position, a methoxy group (-OCH3) at the 2nd carbon position, and a nitro group (-NO2) at the 4th carbon position on a benzene ring. This molecule is a derivative of anisole, with the addition of an ethoxy and nitro group, and is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals. The compound is typically synthesized through a series of chemical reactions, such as nitration and subsequent alkylation, and is used as an intermediate in the production of more complex organic molecules. Its chemical structure and properties make it a versatile building block in organic chemistry, with potential applications in the development of new materials and compounds.

7244-73-7

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7244-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7244-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,4 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7244-73:
(6*7)+(5*2)+(4*4)+(3*4)+(2*7)+(1*3)=97
97 % 10 = 7
So 7244-73-7 is a valid CAS Registry Number.

7244-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethoxy-2-methoxy-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names -

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

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More Details:7244-73-7 SDS

7244-73-7Relevant academic research and scientific papers

TRPV4 ANTAGONISTS

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Page/Page column 42, (2011/10/13)

The present invention relates to quinoline analogs, pharmaceutical compositions containing them and their use as TRPV4 antagonists.

Efficient and practical synthesis of dissymmetrical ethers of 4-nitrocatechol

Subashini, Murugan,Balasubramanian, Kalpattu K.,Bhagavathy, Shanmugasundaram

, p. 3088 - 3106 (2008/12/22)

An efficient and practical synthesis of dissymmetrical ethers of 4-nitrocatechol from 5-nitrosalicyladehyde and 2-hydroxy-5-nitroacetophenone via Baeyer-Villiger oxidation is described. These dissymmetrical ethers are useful in the synthesis of various coccidiostats and other important pharmaceutical intermediates. Copyright Taylor & Francis Group, LLC.

THE NUCLEOPHILIC AROMATIC PHOTOSUBSTITUTION IN PHOTOAFFINITY LABELLING. A MODEL STUDY OF A CYCLOHEXIMIDE DERIVATIVE.

Castello, A.,Marquet, J.,Moreno-Manas, M.,Sirera, X.

, p. 2489 - 2492 (2007/10/02)

The photoreactions of several 4-nitrocatechol ethers with the relatively hard nucleophile methylamine occurs at the meta position respect to the nitro group.A derivative of the antibiotic cycloheximide carrying a 4-nitrocatechol ether moiety reacts with methylamine affording an in vitro model for photoaffinity labelling.

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