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ChemicalBook--->CAS DataBase List--->20691-72-9

20691-72-9

20691-72-9 Structure

20691-72-9 Structure
IdentificationBack Directory
[Name]

4-Iodo-2-nitroaniline
[CAS]

20691-72-9
[Synonyms]

4-Iodo-2-nitroaniline
4-IODO-2-NITROANILINE 97
4-Iodo-2-nitrophenylamine
4-Iodo-2-nitroaniline 98%
2-Amino-5-iodonitrobenzene
Benzenamine, 4-iodo-2-nitro-
4-Iodo-2-nitroaniline
4-Iodo-2-nitroaniline ISO 9001:2015 REACH
[Molecular Formula]

C6H5IN2O2
[MDL Number]

MFCD06808526
[MOL File]

20691-72-9.mol
[Molecular Weight]

264.02
Chemical PropertiesBack Directory
[Melting point ]

120-123 °C(lit.)
[Boiling point ]

352.9±27.0 °C(Predicted)
[density ]

2.101±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

-1.19±0.10(Predicted)
[color ]

Dark Red to Dark Brown
[Stability:]

Air Sensitive
[InChI]

InChI=1S/C6H5IN2O2/c7-4-1-2-5(8)6(3-4)9(10)11/h1-3H,8H2
[InChIKey]

QVCRSYXVWPPBFJ-UHFFFAOYSA-N
[SMILES]

C1(N)=CC=C(I)C=C1[N+]([O-])=O
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-43
[Safety Statements ]

36/37
[WGK Germany ]

2
[HS Code ]

2921490090
Hazard InformationBack Directory
[Uses]

4-Iodo-2-nitroaniline can be used in organic synthesis.
[Synthesis]

2-Nitroaniline

88-74-4

4-Iodo-2-nitroaniline

20691-72-9

The general procedure for the synthesis of 4-iodo-2-nitroaniline from 2-nitroaniline is as follows: iodination in the presence of Na2SO3 (typical procedure). To a 100 mL round bottom flask was added a solution of 3 mmol 2-nitroaniline in 10 mL acetic acid and a solution of KI3 and Na2SO3 prepared in advance by adding 3 mmol iodine and 3 mmol Na2SO3 to the solution. A solution of 3 mmol potassium iodide in 3 mL of water was quickly added. At the same time, a solution of 3 mmol NaIO4 in 5 mL of water was added and 0.5 mL of sulfuric acid was quickly added using a pressure-balanced dropping funnel. The reaction mixture was stirred at 25 °C and the reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was poured into ice-cold water and the solid product, 4-iodo-2-nitroaniline, was isolated by vacuum filtration, washed twice with deionized water and dried under appropriate conditions.

[References]

[1] Monatshefte fur Chemie, 2002, vol. 133, # 10, p. 1325 - 1330
[2] Tetrahedron Letters, 2006, vol. 47, # 28, p. 4793 - 4796
[3] Russian Journal of Organic Chemistry, 2016, vol. 52, # 3, p. 433 - 436
[4] Zh. Org. Khim., 2016, vol. 52, # 3, p. 433 - 436,4
[5] Tetrahedron, 2003, vol. 59, # 14, p. 2497 - 2518
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