ChemicalBook > CAS DataBase List > 5-Nitro-3-(trifluoromethyl)-2-pyridinamine

5-Nitro-3-(trifluoromethyl)-2-pyridinamine

Product Name
5-Nitro-3-(trifluoromethyl)-2-pyridinamine
CAS No.
1121056-94-7
Chemical Name
5-Nitro-3-(trifluoromethyl)-2-pyridinamine
Synonyms
5-Nitro-3-(trifluoroMethyl)pyridin-2-aMine;5-Nitro-3-(trifluoromethyl)-2-pyridinamine;5-Nitro-3-trifluoroMethyl-pyridin-2-ylaMine;2-Pyridinamine, 5-nitro-3-(trifluoromethyl)-
CBNumber
CB12534645
Molecular Formula
C6H4F3N3O2
Formula Weight
207.11
MOL File
1121056-94-7.mol
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5-Nitro-3-(trifluoromethyl)-2-pyridinamine Property

Boiling point:
308℃
Density 
1.589
Flash point:
140℃
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
0.09±0.49(Predicted)
Appearance
Off-white to yellow Solid
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
N900995
Product name
5-Nitro-3-(trifluoromethyl)pyridin-2-amine
Packaging
50mg
Price
$110
Updated
2021/12/16
Matrix Scientific
Product number
093295
Product name
5-Nitro-3-(trifluoromethyl)pyridin-2-amine
Purity
95+%
Packaging
250mg
Price
$473
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
HCH0367523
Product name
5-NITRO-3-(TRIFLUOROMETHYL)PYRIDIN-2-AMINE
Purity
95.00%
Packaging
5MG
Price
$500.52
Updated
2021/12/16
Matrix Scientific
Product number
093295
Product name
5-Nitro-3-(trifluoromethyl)pyridin-2-amine
Purity
95+%
Packaging
1g
Price
$975
Updated
2021/12/16
Ambeed
Product number
A167408
Product name
5-Nitro-3-(trifluoromethyl)pyridin-2-amine
Purity
96%
Packaging
100mg
Price
$45
Updated
2021/12/16
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5-Nitro-3-(trifluoromethyl)-2-pyridinamine Chemical Properties,Usage,Production

Synthesis

183610-70-0

1121056-94-7

General procedure for the synthesis of 5-nitro-3-(trifluoromethyl)pyridin-2-amine from 2-amino-3-(trifluoromethyl)pyridine: 2-amino-3-(trifluoromethyl)pyridine (2 g, 12.34 mmol) was dissolved in concentrated sulfuric acid (10 mL) at 0 °C, and fuming nitric acid (0.56 mL, 12.34 mmol) was slowly added dropwise. After the dropwise addition, the reaction mixture was kept stirred at 0°C for 15 minutes, then brought to room temperature and continued to stir for 1 hour. After that, the reaction system was heated to 50 °C and maintained for 2 hours. Upon completion of the reaction, the mixture was cooled to room temperature and quenched by slowly pouring into ice water (200 mL). The precipitated solid product was collected by filtration and dried under high vacuum to afford 5-nitro-3-(trifluoromethyl)pyridin-2-amine (1.92 g, 75% yield). The structure of the product was confirmed by 1H NMR (d6-DMSO, 300 MHz) δ 8.02 (brs, 2H), 8.38 (d, 1H, J = 2.6 Hz), 9.04 (d, 1H, J = 2.6 Hz) and mass spectrum (ESI) m/z = 208 (MH+).

References

[1] Patent: WO2009/23179, 2009, A2. Location in patent: Page/Page column 240-241

5-Nitro-3-(trifluoromethyl)-2-pyridinamine Preparation Products And Raw materials

Raw materials

Preparation Products

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5-Nitro-3-(trifluoromethyl)-2-pyridinamine Suppliers

Tetranov Biopharm
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