2-AMINO-5-IODOBENZONITRILE

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Products Intro: Product Name:2-Amino-5-iodobenzonitrile
CAS:132131-24-9
Purity:98% (Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:132131-24-9
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CAS:132131-24-9
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CAS:132131-24-9
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Products Intro: Product Name:2-Amino-5-iodobenzonitrile
CAS:132131-24-9
Purity:>97% Package:0.1g;0.25g;1g;5g;10g;25g

2-AMINO-5-IODOBENZONITRILE manufacturers

2-AMINO-5-IODOBENZONITRILE Basic information
Product Name:2-AMINO-5-IODOBENZONITRILE
Synonyms:2-AMINO-5-IODOBENZONITRILE;2-Cyano-4-iodoaniline;2-aminio-5-iodobenzonitrile;5-iodoanthranilonitrile;Benzonitrile, 2-amino-5-iodo-
CAS:132131-24-9
MF:C7H5IN2
MW:244.03
EINECS:
Product Categories:
Mol File:132131-24-9.mol
2-AMINO-5-IODOBENZONITRILE Structure
2-AMINO-5-IODOBENZONITRILE Chemical Properties
Melting point 86℃ (ethanol )
Boiling point 333.6±37.0 °C(Predicted)
density 1.98±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka1.02±0.10(Predicted)
AppearanceOff-white to yellow Solid
Safety Information
MSDS Information
2-AMINO-5-IODOBENZONITRILE Usage And Synthesis
Uses2-Amino-5-iodobenzonitrile is a useful intermediate for the synthesis of lapatinib intermediate of N-[3-chloro-4-3-fluorophenzyloxyphenyl]-6-iodoquinazolin-4-amine.
Synthesis
2-Aminobenzonitrile

1885-29-6

2-AMINO-5-IODOBENZONITRILE

132131-24-9

The general procedure for the synthesis of 2-amino-5-iodobenzonitrile from 2-aminobenzonitrile is as follows: 1. A mixture of 2-aminobenzonitrile (0.02 mol) and ammonium iodide (0.02 mol) was dissolved in acetic acid (50 mL). 2. 30% aqueous hydrogen peroxide (0.13 mol) was added dropwise to the above solution slowly at 30 °C. 3. The reaction mixture was stirred at room temperature for 12 hours. 4. For 12 h. 4. After completion of the reaction, the reaction solution was treated with aqueous sodium thiosulfate (40 mL, 0.03 mol) and the pH was adjusted to about 8 by addition of 20% sodium hydroxide solution. 5. The reaction mixture was continued to be stirred at room temperature for 0.5 h. 6. The partially precipitated 2-amino-5- iodobenzonitrile (Product A) was separated by vacuum filtration to give a silvery-white flaky solid in a yield of 92.6%.

References[1] Acta Crystallographica Section C: Crystal Structure Communications, 2007, vol. 63, # 7, p. o408-o410
[2] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 7, p. 1584 - 1587
[3] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 18, p. 4309 - 4313
[4] Bioorganic and Medicinal Chemistry, 2005, vol. 13, # 7, p. 2637 - 2649
[5] Patent: CN103896889, 2016, B. Location in patent: Paragraph 0041-0043
2-AMINO-5-IODOBENZONITRILE Preparation Products And Raw materials
Raw materialsN-Iodosuccinimide-->2-Aminobenzonitrile
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