63649-64-9

Usage

Uses

Used in Dye and Pigment Industry:
4-ISOPROPYL-2-NITROANILINE is used as a chemical intermediate for the synthesis of various dyes and pigments. Its unique structure allows for the creation of a wide range of colorants used in different applications, including textiles, plastics, and printing inks.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4-ISOPROPYL-2-NITROANILINE is utilized as a precursor in the production of various organic chemicals and pharmaceuticals. Its presence in the synthesis process contributes to the development of new drugs and medicinal compounds, enhancing the range of treatments available for various health conditions.
Used in Organic Chemical Production:
4-ISOPROPYL-2-NITROANILINE is also employed in the synthesis of other organic chemicals. Its versatile chemical structure makes it a valuable component in the creation of specialty chemicals used across various industries, such as agriculture, cosmetics, and materials science.
Safety Precautions:
Given the potential health hazards associated with 4-ISOPROPYL-2-NITROANILINE, it is essential to implement proper safety measures when working with 4-ISOPROPYL-2-NITROANILINE. This includes using appropriate personal protective equipment, ensuring proper ventilation, and adhering to established safety protocols to minimize exposure and mitigate risks.

InChI:InChI=1/C9H12N2O2/c1-6(2)7-3-4-8(10)9(5-7)11(12)13/h3-6H,10H2,1-2H3

Upstream product

• 40655-36-5 N-(4-iso-propyl-2-nitrophenyl)acetamide 
• 1338684-26-6 2,2,2-trifluoro-N-(4-isopropyl-2-nitrophenyl)acetamide 
• 99-88-7 4-Isopropylaniline 
• 5702-74-9 N-(4-iso-propylphenyl)acetamide 

Downstream Products

• 6526-74-5 3-isopropylnitrobenzene 
• 56471-90-0 4-(1-methylethyl)-1,2-benzenediamine 
• 1576-10-9 4-isopropyl-2-nitrophenol 
• 144146-98-5 1-iodo-4-isopropyl-2-nitrobenzene 
• 71462-99-2 4-isopropyl-2-nitrophenyl acetate 
• 618-45-1 3-isopropylhydroxybenzene 
• 6380-20-7 3-isopropylanisole 
• 5369-16-4 meta-iso-propyl aniline 
• 725229-17-4 2-tert-butyl-5-isopropyl-anisole 
• 99758-47-1 6-tert-butyl-3-isopropyl-2,4-dinitro-anisole 
• 103151-03-7 5-isopropyl-1,3-dihydro-benzimidazol-2-one 
• 335254-70-1 (4-isopropyl-2-nitro-phenyl)-carbamic acid tert.-butyl ester 
• 1338685-19-0 N₁-[3-(4-chlorophenyl)-2-isobutoxypropyl]-4-isopropylbenzene-1,2-diamine 
• 1338685-12-3 10-[3-(4-chlorophenyl)-2-isobutoxypropyl]-7-isopropylbenzo[g]pteridine-2,4(3H,10H)-dione 

Relevant academic research and scientific papers

RETRACTED ARTICLE: Room-temperature Cu(II)-catalyzed chemo- and regioselective ortho-nitration of arenes via C-H functionalization

An efficient Cu-catalyzed chemo- and regioselective ortho-nitration of N,1-diaryl-5-aminotetrazoles and N,4-diaryl-3-amino-1,2,4-triazoles has been described with good functional group compatibility. The procedure features the use of an operationally simple protocol utilizing the commercially available less toxic CuCl2·2H2O as catalyst and Fe(NO3)3· 9H2O as nitration source at room temperature. Removal of the 5-aminotetrazole directing group has been demonstrated using base hydrolysis to afford substituted 2-nitroanilines.

Room-Temperature Cu(II)-Catalyzed Chemo- and Regioselective Ortho-Nitration of Arenes via C-H Functionalization

An efficient Cu-catalyzed chemo- and regioselective ortho-nitration of N,1-diaryl-5-aminotetrazoles and N,4-diaryl-3-amino-1,2,4-triazoles have been described with good functional group compatibility. The procedure features the use of operationally simple protocol utilizing the commercially available less toxic CuCl2·2H2O as catalyst and Fe(NO3)3·9H2O as nitration source at room temperature. Removal of the 5-aminotetrazole directing group has been demonstrated using base hydrolysis to afford substituted 2-nitroanilines.

FLAVIN DERIVATIVES

The present invention relates novel flavin derivatives, their use and compositions for use as riboswitch ligands and/or anti-infectives.