29632-73-3

  • Product Name:2-Bromo-4-iodoaniline
  • Molecular Formula:C6H5 Br I N
  • Purity:98% GC
  • Molecular Weight:297.921
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Product Details

Top Quality 2-Bromo-4-iodoaniline 29632-73-3 Hot Sell In Stock

  • Molecular Formula:C6H5 Br I N
  • Molecular Weight:297.921
  • Vapor Pressure:0.001mmHg at 25°C 
  • Melting Point:75-76 ºC 
  • Boiling Point:307.61°C at 760 mmHg 
  • Flash Point:139.838°C 
  • PSA:26.02000 
  • Density:2.292 
  • LogP:3.21710 

2-Bromo-4-iodoaniline(Cas 29632-73-3) Usage

General Description

2-Bromo-4-iodoaniline is a chemical compound consisting of an aniline ring with a bromine and iodine atom attached to it. It is a light yellow to brown solid, and is commonly used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. 2-Bromo-4-iodoaniline is known to be toxic if ingested, inhaled, or absorbed through the skin, and can cause irritation to the respiratory system and skin. It has also been found to have mutagenic and carcinogenic properties, making it a hazardous material that requires careful handling and disposal. Additionally, 2-Bromo-4-iodoaniline may cause environmental harm if released into water or soil. Due to its potentially harmful effects, proper precautions and safety measures should be taken when working with this chemical.

InChI:InChI=1/C6H5BrIN/c7-5-3-4(8)1-2-6(5)9/h1-3H,9H2

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29632-73-3 Process route

2-bromoaniline
615-36-1

2-bromoaniline

2-Bromo-4-iodoaniline
29632-73-3

2-Bromo-4-iodoaniline

4-chloro-2-bromoaniline
873-38-1

4-chloro-2-bromoaniline

Conditions
Conditions Yield
With 1-butyl-3-methyl-pyridinium dichloroiodate; for 1h;
86 %Chromat.
80 %Chromat.
2-bromoaniline
615-36-1

2-bromoaniline

2-Bromo-4-iodoaniline
29632-73-3

2-Bromo-4-iodoaniline

Conditions
Conditions Yield
With N-iodo-succinimide; In dimethyl sulfoxide; at 20 ℃; for 18h;
98%
With 1,4-dibenzyl-1,4-diazoniabicyclo[2.2.2]octane dichloroiodate; In neat (no solvent); at 20 ℃; for 0.333333h; regioselective reaction;
88%
With N,N,N-trimethylbenzenemethanaminium dichloroiodate; calcium carbonate; In methanol; dichloromethane; for 22h;
83%
With [K(18-crown-6)]ICl2; potassium carbonate; In acetonitrile; at 50 ℃; for 12h; regioselective reaction;
72%
With sodium percarbonate; iodine; acetic acid; In ethyl acetate; at 45 - 50 ℃; for 3.5h;
67%
With iodine; periodic acid; In dichloromethane; for 0.333333h; Heating; microwave irradiation;
14%
With sodium hydrogencarbonate; N,N,N-trimethylbenzenemethanaminium dichloroiodate; In methanol; dichloromethane; at 20 ℃; for 0.333333h;
1.34 g
With iodine; sodium hydrogencarbonate; aniline; In water; ethyl acetate;
2.53 g (91%)
With N-iodo-succinimide; In dimethyl sulfoxide; at 20 ℃; for 72h; regioselective reaction;

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