2-Bromo-4-iodoaniline

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Products Intro: Product Name:2-Bromo-4-iodoaniline
CAS:29632-73-3
Purity:98%(MinGC) Package:1G;1KG;100KG
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Products Intro: Product Name:2-Bromo-4-iodoaniline
CAS:29632-73-3
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Products Intro: Product Name:2-Bromo-4-iodoaniline
CAS:29632-73-3
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
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CAS:29632-73-3
Purity:98% Package:1KG;1USD
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2-Bromo-4-iodoaniline manufacturers

  • 2-Bromo-4-iodoaniline
  • 2-Bromo-4-iodoaniline pictures
  • $1.00 / 1KG
  • 2019-07-06
  • CAS:29632-73-3
  • Min. Order: 1KG
  • Purity: 98%
  • Supply Ability: 100KG
2-Bromo-4-iodoaniline Basic information
Product Name:2-Bromo-4-iodoaniline
Synonyms:2-Bromo-4-iodoaniline;2-Bromo-4-iodoanilin;2-Bromo-4-iodobenzenamine;Benzenamine, 2-bromo-4-iodo-
CAS:29632-73-3
MF:C6H5BrIN
MW:297.92
EINECS:
Product Categories:
Mol File:29632-73-3.mol
2-Bromo-4-iodoaniline Structure
2-Bromo-4-iodoaniline Chemical Properties
Melting point 75-76 °C
Boiling point 307.6±32.0 °C(Predicted)
density 2.292
storage temp. Keep in dark place,Inert atmosphere,2-8°C
form tiny crystalline needles
pka1.74±0.10(Predicted)
color Fawn/mauve
Safety Information
HS Code 2921420090
MSDS Information
2-Bromo-4-iodoaniline Usage And Synthesis
Synthesis
2-Bromoaniline

615-36-1

2-Bromo-4-iodoaniline

29632-73-3

Part A. Synthesis of 2-bromo-4-iodoaniline The synthesis of this compound is based on a modified method of J. Chem. Soc., Perkin Trans. 1, 1970, 2106. The specific steps are as follows: 1. 1.61 g (9.36 mmol) of o-bromoaniline was mixed with 10 mL of water and 750 mg of sodium bicarbonate solid was added. 2. Mildly heat the mixture using a hot air gun to melt the aniline. 3. 2.58 g (10.2 mmol) of powdered iodine is added in batches over several minutes. 4. 4. Stir the reaction mixture for 2 hours at room temperature. 5. 5. The resulting dark solid product is collected by filtration, washed with water and dried over air to give a slightly wetted dark solid. 6. The product was purified directly by rapid column chromatography on silica gel, eluting first with hexane and subsequently with a hexane solution containing 5% ethyl acetate to afford 2.53 g (91% yield) of the target compound 2-bromo-4-iodoaniline as a pale pink solid.

References[1] Bulletin of the Chemical Society of Ethiopia, 2015, vol. 29, # 1, p. 157 - 162
[2] Chemical Communications, 2012, vol. 48, # 48, p. 6052 - 6054
[3] Organic and Biomolecular Chemistry, 2011, vol. 9, # 8, p. 2987 - 2991
[4] Molecules, 2005, vol. 10, # 10, p. 1307 - 1317
[5] Molecules, 2004, vol. 9, # 7, p. 617 - 621
2-Bromo-4-iodoaniline Preparation Products And Raw materials
Raw materials2-Bromoaniline-->4-Iodoaniline-->Ethyl acetate-->Aniline-->iodine-->Sodium bicarbonate
Tag:2-Bromo-4-iodoaniline(29632-73-3) Related Product Information
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