64123-46-2

Usage

Molecular weight

195.21 g/mol

Structure

A benzene ring with a nitro group (-NO2) and a methoxymethyl (-OCH2-) group attached at the ortho position, and an ethyl group (-C2H5) attached at the meta position

Physical properties

Pale yellow solid, slightly soluble in water, soluble in organic solvents

Uses

Intermediate in the synthesis of pharmaceuticals and agrochemicals, precursor in the production of dyes and pigments, potential use in the production of polymers and as a chemical intermediate in the manufacturing of various other organic compounds.

InChI:InChI=1/C10H13NO3/c1-3-8-4-5-10(11(12)13)6-9(8)7-14-2/h4-6H,3,7H2,1-2H3

Upstream product

• 22490-32-0 3-chloromethyl-4-ethylnitrobenzene 
• 100-12-9 4-ethylnitrobenzene 
• 124-41-4 sodium methylate 

Downstream Products

• 64123-01-9 (3-Chloro-1-methyl-propyl)-(4-ethyl-3-methoxymethyl-2,6-dinitro-phenyl)-amine 
• 64122-90-3 (4-Ethyl-3-methoxymethyl-2,6-dinitro-phenyl)-propyl-amine 
• 64123-48-4 4-ethyl-N-(1-ethylpropyl)-α-methoxy-2,6-dinitro-m-toluidine 
• 64122-98-1 Allyl-(4-ethyl-3-methoxymethyl-2,6-dinitro-phenyl)-amine 
• 64123-47-3 4-ethyl-N-(1-ethylpropyl)-α-methoxy-m-toluidine 
• 64122-99-2 (2-Chloro-1-methyl-ethyl)-(4-ethyl-3-methoxymethyl-2,6-dinitro-phenyl)-amine 
• 69886-08-4 1-Ethyl-4-amino-2-methoxymethylbenzol 

Relevant academic research and scientific papers

2,6-Dinitroaniline herbicides

The invention is the use of substituted 2,6-dinitroaniline compounds as preemergence herbicides and compositions employing the substituted 2,6-dinitroaniline compounds.

2,6-Dinitroaniline herbicides

This invention is novel substituted 2,6-dinitroaniline compounds and preemergence herbicidal methods and compositions employing the substituted 2,6-dinitroaniline compounds.

N-alkoxyalkyl-2,6-dinitroaniline herbicides

The invention is substituted 2,6-dinitroaniline compounds and preemergence herbicidal methods and compositions employing the substituted 2,6-dinitroaniline compounds.