ChemicalBook--->CAS DataBase List--->52692-09-8

52692-09-8

52692-09-8 Structure

52692-09-8 Structure
IdentificationBack Directory
[Name]

4-Iodo-2-nitroanisole
[CAS]

52692-09-8
[Synonyms]

4-IODO-2-NITROANISOLE
4-iodo-1-methoxy-2-nitrobenzene
Benzene, 4-iodo-1-methoxy-2-nitro-
[Molecular Formula]

C7H6INO3
[MDL Number]

MFCD08060933
[MOL File]

52692-09-8.mol
[Molecular Weight]

279.03
Chemical PropertiesBack Directory
[Melting point ]

96-98°C
[Boiling point ]

330.8±27.0 °C(Predicted)
[density ]

1.893±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C, protect from light
[Appearance]

Light yellow to yellow Solid
[Sensitive ]

Light Sensitive
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Warning
[Hazard statements ]

H301-H315-H319-H335
[Precautionary statements ]

P261-P280a-P301+P310a-P305+P351+P338-P405-P501a
[Risk Statements ]

23/24/25
[Safety Statements ]

36/37-45
[HS Code ]

2909309090
Hazard InformationBack Directory
[Synthesis Reference(s)]

Tetrahedron Letters, 10, p. 2427, 1969 DOI: 10.1017/S0009838800024678
[Synthesis]

2-Nitroanisole

91-23-6

4-Iodo-2-nitroanisole

52692-09-8

General procedure for the synthesis of 4-iodo-2-nitroanisole from 2-nitroanisole: To a stirred solution of 2-nitroanisole (1 mmol) in dichloromethane (CH2Cl2) or 1,2-dichloroethane ((CH2Cl)2) (0.1 M) was added sequentially Ph3PAuNTf2 (0.025 mmol, 19 mg; if using the 2:1 complex of Ph3PAuNTf2 with toluene) and N-iodosuccinimide (NIS, 1.1 mmol, 248 mg). The reaction mixture was stirred at room temperature or reacted under reflux conditions until complete conversion of the feedstock was confirmed by thin layer chromatography (TLC) monitoring. Upon completion of the reaction, the solvent was evaporated under reduced pressure and the resulting crude product was purified by fast column chromatography using different ratios of hexane and ethyl acetate (EtOAc) as eluents, resulting in pure 4-iodo-2-nitroanisole.

[References]

[1] Synlett, 2014, vol. 25, # 3, p. 399 - 402
[2] Journal of Organic Chemistry, 1990, vol. 55, # 11, p. 3552 - 3555
[3] Tetrahedron, 2004, vol. 60, # 41, p. 9113 - 9119
[4] Synthetic Communications, 2007, vol. 37, # 8, p. 1259 - 1265
[5] Synthesis, 2006, # 7, p. 1195 - 1199
Spectrum DetailBack Directory
[Spectrum Detail]

4-Iodo-2-nitroanisole(52692-09-8)1HNMR
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