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Chemical Structure| 1253383-91-3 Chemical Structure| 1253383-91-3

Structure of 1253383-91-3

Chemical Structure| 1253383-91-3

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Product Details of [ 1253383-91-3 ]

CAS No. :1253383-91-3
Formula : C8H8FNO2
M.W : 169.15
SMILES Code : O=C(OC)C1=CN=C(C)C(F)=C1
MDL No. :MFCD18803129
InChI Key :ZFIHBTMALUQXAL-UHFFFAOYSA-N
Pubchem ID :57516328

Safety of [ 1253383-91-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1253383-91-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1253383-91-3 ]

[ 1253383-91-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1253383-91-3 ]
  • [ 932705-78-7 ]
YieldReaction ConditionsOperation in experiment
800 mg With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20℃; for 1h; To a solution of methyl 5-fluoro-6-methylnicotinate (D16 2.3 g) in THF (10 mL) and methanol (10 mL) was added a solution of NaOH (0.707 g) in water (5 mL) . The mixture was stirred at RT for 1 hour and then concentrated under vacuum. To the residue was added water (5 mL) . The pH of the mixture was adjusted to 3. The solid was collected and dried under vacuum to afford the title compound (800 mg) as a white solid.1H NMR (400 MHz DMSO-d6) 8.83 (s 1H) 8.00 (dd J1.2 Hz 9.6 Hz 1H) 2.57 (s 3H) . MS (ESI) C7H6FNO2requires 155 found 156 [M+H]+.
800 mg With sodium hydroxide; In tetrahydrofuran; methanol; water; at 20℃; for 1h; To a solution of methyl 5-fluoro-6-methylnicotinate (1)18, 2.3 g) in TifF (10 mL) and methanol (10mL) was added a solution of NaOH (0.707 g) in water (5 mL). The mixture was stirred at RT for 1hour, and then concentrated under vacuum. To the residue was added water (5 mL). The pH of themixture was adjusted to 3. The solid was collected and dried under vacuum afford the titlecompound (800 mg) as white solid. ‘H NMR (400 MHz, DMSO-d6): 8.83 (s, 111), 8.00 (dd, J= 1.2 Hz, 9.6 Hz, 1H), 2.57 (s, 3H). MS (ESI): C7H6FNO2 requires 155; found 156 [M+H].
800 mg With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20℃; for 1h; Description 1135-Fluoro-6-methylnicotinic acid (D113) To a solution of methyl 5-fluoro-6-methylnicotinate (Dl 12, 2.3 g) in THF (10 mL) and methanol (10 mL) was added a solution of NaOH (0.707 g) in water (5 mL). The mixture was stirred at RT for 1 hour, and then concentrated under vacuum. To the residue was added water (5 ml). The pH ofthe mixture was adjusted to 3. The solid was collected and dried under vacuum to afford the title compound (800 mg) as white solid. ‘H NMR (400 MHz, DMSO-d6): 8.83 (s, 1H), 8.00 (dd, J= 9.6, 1.2 Hz, 1H), 2.57 (s, 311). MS (ESI): C7H6FNO2 requires 155; found 156 {M+H].
800 mg With water; sodium hydroxide; In tetrahydrofuran; methanol; at 20℃; for 1h; In the containment5-fluoro-6-methylnicotinic acid methyl ester (D16, 2.3 g)Of THF (10 mL) with methanol (10 mL)A solution of NaOH (0.707 g) in water (5 mL) was added to the solution.The mixture was stirred at room temperature for 1 hour,Then concentrated in vacuo. Add water (5 mL) to the residue.Adjust the pH of the mixture to 3.Collect solid, vacuum dry,To give the title compound (800 mg) as a white solid
To a suspension of 5-fluoro-6-methyl-nicotinic acid methyl ester (0.21 g, 1.24 mmol) in a 1:1 mixture of MeOH: water (20 mL) is added sodium hydroxide as a 10% aqueous solution (1.0 mL, 2.5 mmol). The mixture is heated to 50 0C for 1 h then cooled to room temperature and concentrated under reduced pressure to remove volatile organics. The pH of the resulting solution is adjusted to slightly acidic (approximately pH 5) by the addition of a 2N solution of HCl. The mixture is extracted with EtOAc and the combined organic phase is dried over anhydrous sodium sulfate and concentrated to provide 0.170 g of S-fluoro-β-methyl-nicotinic acid as a solid.

 

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