ChemicalBook--->CAS DataBase List--->97760-97-9

97760-97-9

97760-97-9 Structure

97760-97-9 Structure
IdentificationBack Directory
[Name]

2-AMINO-5-IODOBENZOTRIFLUORIDE
[CAS]

97760-97-9
[Synonyms]

ASISCHEM Z25859
2-AMINO-5-IODOBENZOTRIFLUORIDE
4-IODO-2-(TRIFLUOROMETHYL)ANILINE
2-Amino-5-iodobenzotrifluoride98%
2-Amino-5-iodobenzotrifluoride 98%
4-Iodo-2-trifluoromethylphenylamine
2-amino-5-iodo-trifluoromethylbenzene
4-iodo-2-(trifluoromethyl)benzenamine
Benzenamine, 4-iodo-2-(trifluoromethyl)-
2-AMino-5-iodobenzotrifluoride[4-iodo-2-(trifluoroMethyl)aniline]
4-Iodo-2-(trifluoromethyl)aniline, 4-Iodo-alpha,alpha,alpha-trifluoro-o-toluidine
[Molecular Formula]

C7H5F3IN
[MDL Number]

MFCD04972657
[MOL File]

97760-97-9.mol
[Molecular Weight]

287.02
Chemical PropertiesBack Directory
[Boiling point ]

262℃
[density ]

1.948
[Fp ]

112℃
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

liquid
[pka]

0.67±0.10(Predicted)
[color ]

Clear, brown
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P271-P260-P280
[Hazard Codes ]

Xi
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

26-36/37/39
[HazardClass ]

IRRITANT
[HS Code ]

2921420090
Hazard InformationBack Directory
[Uses]

4-Iodo-2-trifluoromethylaniline
[Synthesis]

1-TrifluoroMethyl-1,2-benziodoxol-3(1H)-one

887144-94-7

4-Iodoaniline

540-37-4

2-AMINO-5-IODOBENZOTRIFLUORIDE

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
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMINO-5-IODOBENZOTRIFLUORIDE(97760-97-9)1HNMR
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