41864-45-3

Usage

Uses

Used in Organic Synthesis:
4,5-Dimethoxy-2-methylaniline is used as a chemical intermediate for the synthesis of various organic compounds. Its reactive nature allows it to participate in a range of chemical reactions, making it a valuable component in the creation of new molecules.
Used in Chemical Research:
4,5-Dimethoxy-2-methylaniline is used as a research compound in the field of chemistry. Its unique structure and properties make it an interesting subject for study, particularly in the exploration of new reaction pathways and the development of novel synthetic methods.
Used in Pharmaceutical Industry:
4,5-Dimethoxy-2-methylaniline is used as a building block in the synthesis of certain pharmaceutical compounds. Its presence in the molecular structure can contribute to the overall activity and efficacy of the final drug product.
Used in Dye Industry:
4,5-Dimethoxy-2-methylaniline is used as a precursor in the production of dyes and pigments. Its chemical properties can be exploited to create a variety of colors and shades, making it a useful component in the dye industry.

InChI:InChI=1/C9H13NO2/c1-6-4-8(11-2)9(12-3)5-7(6)10/h4-5H,10H2,1-3H3

Upstream product

• 7509-11-7 1,2-dimethoxy-4-methyl-5-nitrobenzene 

Downstream Products

• 749819-92-9 4-amino-5-methyl-pyrocatechol 
• 860369-12-6 4-Amino-2-methoxy-5-methyl-phenol 
• 856181-38-9 5-Amino-2-methoxy-4-methyl-phenol 
• 408509-80-8 4,5-dimethoxy-N,2-dimethylaniline 
• 58814-69-0 4,5-dimethoxy-2-methyl-benzonitrile 
• 614-13-1 2-methoxy-5-methyl-1,4-benzoquinone 
• 101599-65-9 N-(4,5-Dimethoxy-2-methyl-phenyl)-imino-bernsteinsaeure-diethylester 
• 28046-47-1 N,N'-Bis-4,5-dimethoxy-o-tolyloxamid 
• 30072-80-1 N-(2-Diethylamino-ethyl)-N-(4,5-dimethoxy-2-methyl-phenyl)-N',N'-diethyl-ethane-1,2-diamine 
• 500766-29-0 N₄-(5-tert-butylisoxazol-3-yl)-N₂-(4,5-dimethoxy-2-methyl-phenyl)-pyrimidine-2,4-diamine 
• 500766-44-9 N₂-(2-methyl-4,5-dimethoxyphenyl)-N₄(5-phenylisoxazol-3-yl)-2,4-pyrimidinediamine 
• 438248-93-2 4-(4,5-Dimethoxy-2-methylanilino)-2-(3-pyridinyl)-6-(trifluoromethyl)pyrimidine 
• 1263473-70-6 4-(4-fluoro-phenyl)-1-(2-hydroxy-ethyl)-2-oxo-1,2,3,4-tetrahydro-pyrimidine-5-carboxylic acid (4,5-dimethoxy-2-methyl-phenyl)-amide 

Relevant academic research and scientific papers

Synthesis of 6-methyl-8H-dibenzo[a,g]quinolizin-8-imines via Reissert compounds

Alkylation of Reissert compounds derived from 3-methylisoquinolines with several 2-cyanobenzylbromides followed by hydrolytic cleavage provided the corresponding 1-benzyl-3-methylisoquinolines. Treatment of the latter with methylmagnesiumiodide caused cyclization to the title compounds rather than formation of 2-acetylbenzylisoquinolines.

Multisubstituted 1-hydroxy-9-acridones with anticancer activity

The present invention provides a compound having the structure: STR1 The present invention also provides a method for synthesizing a compound having the above-identified structure as well as the intermediate compounds produced according to that method. The present invention further provides a pharmaceutical composition comprising the above compounds. Lastly, the present invention provides a method of inhibiting growth of tumor cells.