6526-72-3

  • Product Name:1-Isopropyl-2-nitrobenzene
  • Molecular Formula:C9H11NO2
  • Purity:99%
  • Molecular Weight:165.192
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Product Details;

CasNo: 6526-72-3

Molecular Formula: C9H11NO2

factory and supplier 6526-72-3 1-Isopropyl-2-nitrobenzene in stock

  • Molecular Formula:C9H11NO2
  • Molecular Weight:165.192
  • Vapor Pressure:0.0248mmHg at 25°C 
  • Melting Point:-9.5°C 
  • Refractive Index:1.533 
  • Boiling Point:256.4 °C at 760 mmHg 
  • Flash Point:108.5 °C 
  • PSA:45.82000 
  • Density:1.091 g/cm3 
  • LogP:3.24140 

2-NITROCUMENE(Cas 6526-72-3) Usage

General Description

2-Nitrocumene is a nitroalkene compound with the chemical formula C9H9NO2. It is a colorless to pale yellow liquid with a strong, sweet odor. 2-Nitrocumene is used in the production of various chemicals and is also used as a stabilizer and intermediate in the manufacturing of dyes, pharmaceuticals, and pesticides. It is considered to be a hazardous substance and should be handled with care due to its potential toxicity and flammability. Additionally, exposure to 2-Nitrocumene can cause irritation to the skin, eyes, and respiratory system, and ingestion or inhalation of the compound can lead to more serious health effects. Therefore, it is important to follow proper safety precautions and handling procedures when working with 2-Nitrocumene.

InChI:InChI=1/C9H11NO2/c1-7(2)8-5-3-4-6-9(8)10(11)12/h3-7H,1-2H3

6526-72-3 Relevant articles

Telescoped Sequence of Exothermic and Endothermic Reactions in Multistep Flow Synthesis

Sharma, Yachita,Nikam, Arun V.,Kulkarni, Amol A.

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A multistep sequential flow synthesis of...

Regioselective mononitration of aromatic compounds with N2O5 by acidic ionic liquids via continuous flow microreactor

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We employed N2O5 as highly active nitrat...

Efficient synthesis of sterically hindered arenes bearing acyclic secondary alkyl groups by suzuki-miyaura cross-couplings

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Bismuth triflate catalyzed mononitration of aromatic compounds with N 2O5

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6526-72-3 Process route

Isopropylbenzene
98-82-8

Isopropylbenzene

nitro acetate
591-09-3

nitro acetate

4-nitrocumene
1817-47-6

4-nitrocumene

o-nitrocumene
6526-72-3

o-nitrocumene

Conditions
Conditions Yield
Isopropylbenzene
98-82-8

Isopropylbenzene

4-nitrocumene
1817-47-6

4-nitrocumene

o-nitrocumene
6526-72-3

o-nitrocumene

Conditions
Conditions Yield
With nitric acid; acetic anhydride; acetic acid;
With copper(II) nitrate; K10 clay; In acetic anhydride; for 2h; Yield given. Yields of byproduct given; Ambient temperature;
With nitric acid; zeolite beta-I; In 1,2-dichloro-ethane;
With In(OSO2CF3)3; nitric acid; at 20 - 60 ℃; for 24h; Title compound not separated from byproducts;
With nitric acid; ytterbium(III) pefluorooctanesulfonate; lithium perchlorate; molybdenum trioxide; at 60 ℃; for 48h; Title compound not separated from byproducts.;
With trifluoromethylsulfonic anhydride; ethylammonium nitrate; at -5 - 20 ℃; for 0.666667h; Inert atmosphere;
14 %Chromat.
83 %Chromat.
With molybdenum(VI)oxide-silica acidic catalyst; dinitrogen pentoxide; In dichloromethane; at 0 ℃; for 1h; regioselective reaction;
With dinitrogen pentoxide; neodymium(III) trifluoromethanesufonate; In dichloromethane; toluene; at 20 ℃; for 1h;
24.8 %Chromat.
70.2 %Chromat.
With dinitrogen pentoxide; In dichloromethane; at 20 ℃; for 0.5h;
79.6 %Chromat.
16.8 %Chromat.
With bismuth (III) nitrate pentahydrate; for 1.5h; Overall yield = 85 %Chromat.; Schlenk technique; Ionic liquid; Inert atmosphere; Heating;
With bismuth(lll) trifluoromethanesulfonate; dinitrogen pentoxide; In dichloromethane; at 0 ℃; for 2h; Overall yield = 96 %; Green chemistry;
With nitric acid; at 10 ℃; for 0.166667h; Overall yield = 99.6 %Chromat.; Flow reactor;
79 %Chromat.
19.5 %Chromat.

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