2-Trifluoromethyl-6-pyridinecarboxylic acid
2-Trifluoromethyl-6-pyridinecarboxylic acid Basic information
- Product Name:
- 2-Trifluoromethyl-6-pyridinecarboxylic acid
- Synonyms:
-
- 2-TRIFLUOROMETHYL-6-PYRIDINECARBOXYLIC ACID
- 6-(TRIFLUOROMETHYL)PICOLINIC ACID
- 6-TRIFLUOROMETHYLPYRIDINE-2-CARBOXYLIC ACID
- 6-(Trifluoromethyl)pyridine-2-carboxylic acid 97%
- 6-(Trifluoromethyl)pyridine-2-carboxylicacid97%
- 6-(Trifluoromethyl)picolinic acid, 2-Carboxy-6-(trifluoromethyl)pyridine
- 6-TrifluoroMethyl-2-pyridinecarboxylic acid
- 6-(trifluoroMethyl)pyridin-2-carboxylic acid
- CAS:
- 131747-42-7
- MF:
- C7H4F3NO2
- MW:
- 191.11
- Product Categories:
-
- Building Blocks
- C7 to C8
- Chemical Synthesis
- Heterocyclic Building Blocks
- New Products for Chemical Synthesis
- Carboxylic Acids
- Pyridine series
- Carboxylic Acids
- Pyridines
- Mol File:
- 131747-42-7.mol
2-Trifluoromethyl-6-pyridinecarboxylic acid Chemical Properties
- Melting point:
- 154-158 °C
- Boiling point:
- 263.0±40.0 °C(Predicted)
- Density
- 1.484±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- form
- Solid
- pka
- 3.21±0.10(Predicted)
- color
- Off-white
- InChI
- InChI=1S/C7H4F3NO2/c8-7(9,10)5-3-1-2-4(11-5)6(12)13/h1-3H,(H,12,13)
- InChIKey
- OKBHXGBLXDNJJD-UHFFFAOYSA-N
- SMILES
- C1(C(O)=O)=NC(C(F)(F)F)=CC=C1
- CAS DataBase Reference
- 131747-42-7(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,Xn
- Risk Statements
- 22-36/37/38
- Safety Statements
- 26
- RIDADR
- UN2811
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HazardClass
- 6.1
- HS Code
- 2933399990
2-Trifluoromethyl-6-pyridinecarboxylic acid Usage And Synthesis
Chemical Properties
White powder
Uses
A useful organic intermediate.
Synthesis
124-38-9
189278-27-1
131747-42-7
General procedure for the synthesis of 6-(trifluoromethyl)pyridine-2-carboxylic acid from carbon dioxide and 2-bromo-6-trifluoromethylpyridine: 1. 2-Bromo-6-(trifluoromethyl)pyridine (100 mg, 0.44 mmol, 1 eq.) was dissolved in anhydrous ether at room temperature and protected by nitrogen and subsequently cooled to -70 °C. 2. 1.6 M hexane solution of n-butyllithium (0.28 mL, 0.44 mmol, 1 eq.) was added slowly and dropwise through the addition funnel. 3. The reaction mixture was stirred at -40 °C for 15 minutes and then cooled to -70 °C again. 4. Carbon dioxide gas was introduced into the reaction mixture and continuously bubbled for 10 minutes. 5. Allow the reaction mixture to warm slowly to room temperature. 6. 6. the reaction was terminated by addition of water and subsequently washed three times with ether. 7. Adjust the pH of the aqueous layer to 3 with concentrated hydrochloric acid. 8. Extracted the acidic aqueous layer with ethyl acetate three times. 9. The ethyl acetate layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give 6-(trifluoromethyl)pyridine-2-carboxylic acid (30 mg) as a white solid in 35% yield. 10. The product was detected by LCMS and the molecular ion peak (M + H)+ = 192.06 was confirmed.
References
[1] European Journal of Organic Chemistry, 2003, # 8, p. 1559 - 1568
[2] Patent: US2005/54626, 2005, A1. Location in patent: Page/Page column 36
2-Trifluoromethyl-6-pyridinecarboxylic acid Preparation Products And Raw materials
Raw materials
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2-Trifluoromethyl-6-pyridinecarboxylic acid(131747-42-7)Related Product Information
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- 3-(Trifluoromethyl)benzoic acid
- 2-Picoline
- 2-(Trifluoromethyl)benzoic acid
- 4-(Trifluoromethyl)pyridine
- Zinc picolinate
- 2-Chloro-6-(trifluoromethyl)pyridine
- 6-(trifluoromethyl)picolinic acid
- 2-(difluoromethyl)-5-(4,5-dihydro-2-thiazolyl)-4-(2-methylpropyl-6-trifluoromethyl)-3-pyridinecarboxylic acid methyl ester
- 5-TRIFLUOROMETHYL-2-PYRIDINECARBOXYLIC ACID
- 2-CHLORO-6-TRIFLUOROMETHYL-3-PYRIDINECARBOXYLIC ACID
- 2-Chloro-5-(trifluoromethyl)-3-pyridinecarboxylic acid
- 3-(trifluoromethyl)-2-pyridinecarboxylic acid