609-73-4

  • Product Name:1-Iodo-2-nitrobenzene
  • Molecular Formula:C6H4INO2
  • Purity:99%
  • Molecular Weight:249.008
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Product Details;

CasNo: 609-73-4

Molecular Formula: C6H4INO2

Appearance: solid

factory and supplier 609-73-4 1-Iodo-2-nitrobenzene in stock

  • Molecular Formula:C6H4INO2
  • Molecular Weight:249.008
  • Appearance/Colour:solid 
  • Vapor Pressure:0.00404mmHg at 25°C 
  • Melting Point:49-51 °C(lit.) 
  • Refractive Index:1.663 
  • Boiling Point:288.5 °C at 760 mmHg 
  • Flash Point:122.9 °C 
  • PSA:45.82000 
  • Density:2.018 g/cm3 
  • LogP:2.72260 

1-Iodo-2-nitrobenzene(Cas 609-73-4) Usage

InChI:InChI=1/C6H4INO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H

609-73-4 Relevant articles

Nitration of Phenylboron Dichloride with Nitronium Tetrafluoroborate. Attempted Nitration of Iodobenzene and Phenylphosphorous Dichloride

Olah, George A.,Piteau, Mark,Laali, Khosrow,Rao, Chandra B.,Farooq, Omar

, p. 46 - 48 (1990)

Electrophilic nitration of phenylboron d...

Low-temperature and highly efficient liquid-phase catalytic nitration of chlorobenzene with NO2: Remarkably improving the para-selectivity in O2-Ac2O-Hβ composite system

Deng, Renjie,Liu, Pingle,Luo, He'an,Ni, Wenjin,You, Kuiyi,Zhao, Fangfang

, (2020/02/26)

In this work, we developed a low-tempera...

NITRATION

-

Page/Page column 36; 41; 46; 64; 37; 43; 48; 69, (2020/05/28)

The present invention relates to a proce...

Dehydroxyalkylative halogenation of C(aryl)-C bonds of aryl alcohols

Liu, Mingyang,Zhang, Zhanrong,Liu, Huizhen,Wu, Tianbin,Han, Buxing

supporting information, p. 7120 - 7123 (2020/07/14)

We herein report Cu mediated side-direct...

Arene diazonium saccharin intermediates: A greener and cost-effective alternative method for the preparation of aryl iodide

Ghaffari Khaligh, Nader,Rafie Johan, Mohd,Shahnavaz, Zohreh,Zaharani, Lia

, p. 535 - 542 (2020/06/01)

In the current protocol, the arene diazo...

609-73-4 Process route

iodobenzene
591-50-4

iodobenzene

p-nitrobenzene iodide
636-98-6

p-nitrobenzene iodide

m-iodonitrobenzene
645-00-1

m-iodonitrobenzene

o-nitroiodobenzene
609-73-4

o-nitroiodobenzene

Conditions
Conditions Yield
With silver nitrate; boron trifluoride; In acetonitrile; at 25 ℃; for 10h; Product distribution; competitive nitration benzene, relative rate;
17 % Chromat.
3 % Chromat.
80 % Chromat.
With nitro acetate; H-ZSM-11; In hexane; at 30 ℃; Product distribution; different catalysts;
With Hβ zeolite; oxygen; dinitrogen tetraoxide; In 1,2-dichloro-ethane; at 0 ℃; for 48h; Title compound not separated from byproducts.;
With nitric acid; acetic anhydride; In tetrachloromethane;
With nitrogen dioxide; oxygen; acetic anhydride; at 35 ℃; under 3750.38 Torr; Autoclave;
iodobenzene
591-50-4

iodobenzene

p-nitrobenzene iodide
636-98-6

p-nitrobenzene iodide

o-nitroiodobenzene
609-73-4

o-nitroiodobenzene

Conditions
Conditions Yield
With nitric acid; at 50 ℃; for 3h;
29.2%
70.2%
With trinitratooxovanadium(V); In dichloromethane; for 0.333333h; Ambient temperature;
34%
63%
With trinitratooxovanadium(V); In dichloromethane; for 0.333333h; Ambient temperature;
62%
35%
With iodine; silver nitrate; chloro-diphenylphosphine; In dichloromethane; at 20 ℃; for 24h;
10%
57%
With nitric acid;
With tetrachloromethane; dinitrogen tetraoxide; at 20 ℃;
With tetrachloromethane; aluminium trichloride; dinitrogen tetraoxide; at 0 - 5 ℃;
With dinitrogen tetraoxide; In acetonitrile; at 25 ℃; Product distribution; Kinetics; electrochemical nitration (1.6 V), anode: Pt, cathode: Ni; electrolyte: Et4NBF4; other solvents (MeNO2, CH2Cl2); polarization curves;
With nitric acid; bleibt beim Umkrystallisieren des Reaktionsprodukts aus Alkohol in der Mutterlauge;
With nitric acid; at 0 ℃;
With nitric acid; at -30 ℃;
With nitric acid; zeolite beta-I; In 1,2-dichloro-ethane;
With perchloric acid; montmorillonite K10 supported ammonium nitrate; at 65 ℃; for 1.5h; Title compound not separated from byproducts;
With phosphorus pentoxide; nitric acid; In 1,2-dichloro-ethane; at 40 ℃; for 4h; regioselective reaction;
With lanthanum bis[(trifluoromethyl)sulfonyl]imide; nitric acid; In water; at 85 ℃; for 24h; regioselective reaction; Ionic liquid;
With nitric acid; acetic anhydride; In tetrachloromethane; at 50 ℃; for 2h; regioselective reaction;

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