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3,5-Difluoro-4-iodoaniline

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3,5-Difluoro-4-iodoaniline Basic information

Product Name:
3,5-Difluoro-4-iodoaniline
Synonyms:
  • BUTTPARK 120\07-59
  • 3,5-difluoro-4-iodobenzenamine
  • 3,5-Difluoro-4-iodoaniline 97%
  • 3,5-Difluoro-4-iodoaniline97%
  • 3,5-DIFLUORO-4-IODOANILINE
  • Benzenamine, 3,5-difluoro-4-iodo-
CAS:
1542-34-3
MF:
C6H4F2IN
MW:
255
Mol File:
1542-34-3.mol
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3,5-Difluoro-4-iodoaniline Chemical Properties

Melting point:
112
Boiling point:
270.6±40.0 °C(Predicted)
Density 
2.086±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
1.77±0.10(Predicted)
InChI
InChI=1S/C6H4F2IN/c7-4-1-3(10)2-5(8)6(4)9/h1-2H,10H2
InChIKey
CHXXMQJPYOKYSB-UHFFFAOYSA-N
SMILES
C1(N)=CC(F)=C(I)C(F)=C1
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Safety Information

HS Code 
2921420090
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3,5-Difluoro-4-iodoaniline Usage And Synthesis

Uses

3,5-Difluoro-4-Iodoaniline is a useful research chemical.

Definition

3,5-Difluoro-4-iodoaniline is a halogenated aromatic compound that has a thiol group. It is synthesized by the stepwise alkylation of 3,5-difluoroaniline with ethyl bromoacetate and subsequent deamination with hydrochloric acid. The lithiation process then yields the corresponding lithiated product, which can be iodinated with iodine in acetic acid to give 3,5-difluoro-4-iodoiodobenzenesulfonic acid. The halogenation process involves the treatment of 3,5-difluoro-4-iodoaniline with phosphorus pentachloride to form 3,5-dichloro-4-iodoaniline. Finally, the benzenes are obtained by hydrogenation of the 4th position of this compound.

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