63649-64-9

Basic information

• Product Name: 4-ISOPROPYL-2-NITROANILINE
• Synonyms: BENZENAMINE, 4-(1-METHYLETHYL)-2-NITRO-;BUTTPARK 89\07-12;4-ISOPROPYL-2-NITROANILINE;2-nitro-4-(propan-2-yl)aniline;2-Nitro-4-(prop-2-yl)aniline, 4-Amino-3-nitrocumene
• CAS NO: 63649-64-9
• Molecular Formula: C₉H₁₂N₂O₂
• Molecular Weight: 180.2
• EINECS: 200-589-5
• Mol File: 63649-64-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 36-39
• Boiling Point: 142-144/0.4mm
• Flash Point: 133.5 °C
• Appearance: /
• Density: 1.172 g/cm³
• Vapor Pressure: 0.00137mmHg at 25°C
• Refractive Index: 1.581
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 0.40±0.10(Predicted)
• CAS DataBase Reference: 4-ISOPROPYL-2-NITROANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-ISOPROPYL-2-NITROANILINE(63649-64-9)
• EPA Substance Registry System: 4-ISOPROPYL-2-NITROANILINE(63649-64-9)

Safety Data

• Hazard Codes: T
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 63649-64-9(Hazardous Substances Data)

Usage

General Description

4-ISOPROPYL-2-NITROANILINE is a chemical compound with the molecular formula C9H12N2O2. It is an organic compound that consists of a nitro group and aniline group attached to a central isopropyl group. This yellowish crystalline solid is commonly used as an intermediate in the synthesis of various dyes and pigments. It is also used in the production of pharmaceuticals and other organic chemicals. 4-ISOPROPYL-2-NITROANILINE may pose health hazards if not handled properly, and it is important to use proper safety precautions when working with this compound.

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

• 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 
• 40655-36-5 N-(4-iso-propyl-2-nitrophenyl)acetamide 

Downstream Products

• 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 
• 1338685-18-9 N-[3-(4-chlorophenyl)-2-isobutoxypropyl]-4-isopropyl-2-nitroaniline 
• 1338684-27-7 N-[3-(4-chlorophenyl)-2-methylpropyl]-4-isopropyl-2-nitroaniline 
• 1374771-81-9 4-((2-(4-(6-isopropyl-1H-benzo[d]imidazol-2-yl)piperazin-1-yl)pyridin-3-yloxy)methyl)pyrimidin-2-amine 
• 1374771-55-7 2-chloro-6-isopropyl-1H-benzo[d]imidazole 
• 335254-70-1 (4-isopropyl-2-nitro-phenyl)-carbamic acid tert.-butyl ester 
• 103151-03-7 5-isopropyl-1,3-dihydro-benzimidazol-2-one 
• 99758-47-1 6-tert-butyl-3-isopropyl-2,4-dinitro-anisole 
• 725229-17-4 2-tert-butyl-5-isopropyl-anisole 
• 5369-16-4 meta-iso-propyl aniline 
• 6380-20-7 3-isopropylanisole 
• 618-45-1 3-isopropylhydroxybenzene 
• 71462-99-2 4-isopropyl-2-nitrophenyl acetate 

Relevant articles and documents

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.

FLAVIN DERIVATIVES

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