ChemicalBook--->CAS DataBase List--->5399-03-1

5399-03-1

5399-03-1 Structure

5399-03-1 Structure
IdentificationMore
[Name]

2-Iodo-4-nitroanisole
[CAS]

5399-03-1
[Synonyms]

2-IODO-4-NITROANISOLE
2-Iodo-4-nitroanisol
Benzene, 2-iodo-1-methoxy-4-nitro-
2-IODO-1-METHOXY-4-NITROBENZENE
[EINECS(EC#)]

611-079-1
[Molecular Formula]

C7H6INO3
[MDL Number]

MFCD00024328
[Molecular Weight]

279.03
[MOL File]

5399-03-1.mol
Chemical PropertiesBack Directory
[Melting point ]

96-98°C
[Boiling point ]

343.3±27.0 °C(Predicted)
[density ]

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

Keep in dark place,Sealed in dry,Room Temperature
[Appearance]

Light brown to brown Solid
[InChI]

InChI=1S/C7H6INO3/c1-12-7-3-2-5(9(10)11)4-6(7)8/h2-4H,1H3
[InChIKey]

KBQBNJHOTNIGDD-UHFFFAOYSA-N
[SMILES]

C1(OC)=CC=C([N+]([O-])=O)C=C1I
[CAS DataBase Reference]

5399-03-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2909309090
Hazard InformationBack Directory
[Uses]

2-Iodo-4-nitroanisole is commonly used in organic synthesis, especially as a synthetic intermediate in the fields of medicine and chemical research.
[Synthesis]

2-Amino-4-nitro anisidine

99-59-2

2-Iodo-4-nitroanisole

5399-03-1

Step A. Synthesis of 2-iodo-1-methoxy-4-nitrobenzene 2-Methoxy-5-nitroaniline (10.0 g, 0.060 mol) was suspended in water (150 mL) and concentrated sulfuric acid (12 mL, 0.22 mol) was added slowly. The temperature of the reaction mixture was maintained below 5 °C under cooling in an ice-salt bath, and a solution of sodium nitrite (4.8 g, 0.070 mol) in water (40 mL) was added dropwise. Subsequently, potassium iodide (16.8 g, 0.101 mol) was added and the mixture was heated to 90 °C and kept for 1 hour. Upon completion of the reaction, it was cooled to 0 °C and deep red crystals were precipitated, which were filtered, washed with water and dried. Purification by silica gel column chromatography (eluent: ethyl acetate/hexane) afforded the target compound 2-iodo-1-methoxy-4-nitrobenzene (13.6 g, 75% yield). 1H NMR (300 MHz, DMSO-d6): δ 8.57 (s, 1H), 8.28 (d, 1H), 7.19 (d, 1H), 3.98 (s, 3H). LCMS (M + H)+: m/z = 280.1 (C7H7INO3).

[References]

[1] Canadian Journal of Chemistry, 2005, vol. 83, # 3, p. 213 - 219
[2] Patent: US2009/286778, 2009, A1. Location in patent: Page/Page column 79
[3] Chem. News J. Ind. Sci., 1901, vol. 83, p. 285
[4] Journal of the Chemical Society, 1901, vol. 79, p. 1076,1077
[5] P. Ch. S., p. 238
Spectrum DetailBack Directory
[Spectrum Detail]

2-Iodo-4-nitroanisole(5399-03-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

5399-03-1(sigmaaldrich)
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