Basic information Safety Supplier Related

2-AMINO-5-IODOBENZOTRIFLUORIDE

Basic information Safety Supplier Related

2-AMINO-5-IODOBENZOTRIFLUORIDE Basic information

Product Name:
2-AMINO-5-IODOBENZOTRIFLUORIDE
Synonyms:
  • 4-IODO-2-(TRIFLUOROMETHYL)ANILINE
  • 2-AMINO-5-IODOBENZOTRIFLUORIDE
  • ASISCHEM Z25859
  • 2-Amino-5-iodobenzotrifluoride 98%
  • 2-Amino-5-iodobenzotrifluoride98%
  • 4-Iodo-2-(trifluoromethyl)aniline, 4-Iodo-alpha,alpha,alpha-trifluoro-o-toluidine
  • 2-AMino-5-iodobenzotrifluoride[4-iodo-2-(trifluoroMethyl)aniline]
  • 2-amino-5-iodo-trifluoromethylbenzene
CAS:
97760-97-9
MF:
C7H5F3IN
MW:
287.02
Product Categories:
  • Phenyls & Phenyl-Het
  • Amines
  • Phenyls & Phenyl-Het
Mol File:
97760-97-9.mol
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2-AMINO-5-IODOBENZOTRIFLUORIDE Chemical Properties

Boiling point:
262℃
Density 
1.948
Flash point:
112℃
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
form 
liquid
pka
0.67±0.10(Predicted)
color 
Clear, brown
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20/21/22-36/37/38
Safety Statements 
26-36/37/39
HazardClass 
IRRITANT
HS Code 
2921420090
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2-AMINO-5-IODOBENZOTRIFLUORIDE Usage And Synthesis

Uses

4-Iodo-2-trifluoromethylaniline

Synthesis

887144-94-7

540-37-4

97760-97-9

The general procedure for synthesizing 2-amino-5-iodobenzotrifluoride from 1-(trifluoromethyl)-1,2-phenyliodonyl-3(1H)-one and p-iodoaniline is as follows: in this embodiment, p-iodoaniline was used as the aromatic amine, and the rest of the reaction conditions and post-processing steps were the same as in Example 28. The specific reaction conditions were as follows: 1-(trifluoromethyl)-1,2-phenyliodono-3(1H)-one (0.5 mmol, 1.0 eq.), p-iodoaniline (1.5 mmol, 3.0 eq.), nickel hydroxide (10 μmol), and potassium carbonate (1.5 mmol, 3.0 eq.) were used as bases, and DMSO (2 mL) was used as a solvent, and the temperature of the reaction was 35 °C. The reaction time was 2 hours. After the reaction was completed, post-treatment was carried out according to the method of Example 1.

References

[1] Organic Letters, 2018, vol. 20, # 13, p. 3732 - 3735
[2] Patent: CN108503552, 2018, A. Location in patent: Paragraph 0240-0244
[3] Patent: CN103553857, 2016, B. Location in patent: Paragraph 0021-0022
[4] Organic Letters, 2014, vol. 16, # 6, p. 1768 - 1771

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