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2-Chloro-4-iodoaniline

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2-Chloro-4-iodoaniline Basic information

Product Name:
2-Chloro-4-iodoaniline
Synonyms:
  • 2-Chloro-4-iodoanili
  • 2-Chloro-4-iodo-benzenaMine
  • NSC 137040
  • 2-Chloro-4-iodoanilline
  • 2-Chloro-4-iodoaniline 97%
  • 2-Chloro-4-iodoaniline, 98% 5GR
  • 2-CHLORO-4-IODOANILINE
  • 2-Chloro-4-iodo-phenylamine
CAS:
42016-93-3
MF:
C6H5ClIN
MW:
253.47
EINECS:
628-520-9
Product Categories:
  • Aromatics
  • Miscellaneous Reagents
  • Aromatic Halides (substituted)
  • Anilines, Amides & Amines
  • C2 to C6
  • Nitrogen Compounds
  • Chlorine Compounds
  • Iodine Compounds
  • Amines
Mol File:
42016-93-3.mol
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2-Chloro-4-iodoaniline Chemical Properties

Melting point:
70-73 °C (lit.)
Boiling point:
281.7±25.0 °C(Predicted)
Density 
1.9011 (estimate)
storage temp. 
Refrigerated.
solubility 
DMSO (Slightly), Methanol (Slightly)
pka
1.86±0.10(Predicted)
form 
powder to crystal
color 
Light yellow to Brown to Dark green
Sensitive 
Light Sensitive
BRN 
2081106
CAS DataBase Reference
42016-93-3(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T,N,Xi,Xn
Risk Statements 
25-37/38-41-51/53-36/37/38-20/21/22
Safety Statements 
26-36/37-45-60-61-36/37/39
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
HazardClass 
6.1
PackingGroup 
III
HS Code 
29214200

MSDS

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2-Chloro-4-iodoaniline Usage And Synthesis

Chemical Properties

grey to light orange crystalline powder

Uses

2-Chloro-4-iodoaniline is a chemical compound that has been synthesized for use as a reagent. It has been used to produce the drug cobimetinib, which is used in the treatment of cancer. 2-Chloro-4-iodoaniline can be prepared by reaction of magnesium with 2-chloroacetaldehyde and nitric acid. This reagent is also useful for preparing Grignard reagents. 2-Chloro-4-iodoaniline can be used to deaminate ketones, nitrates, and chlorides in high yield. 2,4,6-trichlorophenylalanine is an organic compound that contains all three functional groups: a chloride group, a ketone group, and an amino group. The chlorinated carbon atom of the chloride group makes it a good nucleophile and electrophile.

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