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2-(trifluoromethoxy)nicotinic acid

Product Name
2-(trifluoromethoxy)nicotinic acid
CAS No.
1221171-92-1
Chemical Name
2-(trifluoromethoxy)nicotinic acid
Synonyms
2-(trifluoromethoxy)nicotinic acid;3-Pyridinecarboxylic acid, 2-(trifluoromethoxy)-
CBNumber
CB73365473
Molecular Formula
C7H4F3NO3
Formula Weight
207.11
MOL File
1221171-92-1.mol
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2-(trifluoromethoxy)nicotinic acid Property

storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

AK Scientific
Product number
6863CY
Product name
2-(Trifluoromethoxy)nicotinicacid
Packaging
1g
Price
$600
Updated
2021/12/16
AK Scientific
Product number
6863CY
Product name
2-(Trifluoromethoxy)nicotinicacid
Packaging
5g
Price
$1712
Updated
2021/12/16
Chemenu
Product number
CM248305
Product name
2-(Trifluoromethoxy)pyridine-3-carboxylicacid
Purity
95%
Packaging
1g
Price
$1356
Updated
2021/12/16
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2-(trifluoromethoxy)nicotinic acid Chemical Properties,Usage,Production

Synthesis

1221171-91-0

1221171-92-1

General procedure for the synthesis of 2-(trifluoromethoxy)pyridine-3-carboxylic acid from 6-chloro-2-(trifluoromethoxy)nicotinic acid: palladium catalyst (10% loaded on charcoal, 450 mg) was added to a solution of 6-chloro-2-(trifluoromethoxy)nicotinic acid (37,1.5 g, 6.2 mmol) and ammonium formate (790 mg, 12.4 mmol, 2.0 equivalent) in a solution of methanol (10 mL). The reaction mixture was stirred at 55 °C for 16 hours. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated by rotary evaporation. The residue was extracted by partitioning between ethyl acetate (2 x 20 mL) and 2.0 M hydrochloric acid (30 mL). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and the solvent evaporated to give pure 2-(trifluoromethoxy)pyridine-3-carboxylic acid (38,1.05 g, 5.0 mmol, 81% yield) as a white powder with a melting point of 82-85 °C. The product was structurally confirmed by 1H NMR (CD3OD, 300 MHz), 19F NMR ((CD3)2CO, 282 MHz) and 13C NMR (CD3OD, 75 MHz), and elemental analysis was performed (C7H4F3NO3, calculated value: C 40.59%, H 1.95%, N 6.76%; measured value: C 40.35%, H 2.03%, N 6.65%) to verify the purity.

References

[1] European Journal of Organic Chemistry, 2010, # 31, p. 6043 - 6066
[2] Patent: WO2010/40461, 2010, A1. Location in patent: Page/Page column 42

2-(trifluoromethoxy)nicotinic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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2-(trifluoromethoxy)nicotinic acid Suppliers

Tetranov Biopharm
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13526569071
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Bide Pharmatech Ltd.
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Dayang Chem (Hangzhou) Co.,Ltd.
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Career Henan Chemica Co
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Energy Chemical
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1221171-92-1, 2-(trifluoromethoxy)nicotinic acidRelated Search:


  • 2-(trifluoromethoxy)nicotinic acid
  • 3-Pyridinecarboxylic acid, 2-(trifluoromethoxy)-
  • 1221171-92-1