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Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate

CAS No.
1401162-80-8
Chemical Name:
Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate
Synonyms
Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate;2-Pyrimidinecarboxylic acid, 4-(4-fluorophenyl)-, methyl ester
CBNumber:
CB33066455
Molecular Formula:
C12H9FN2O2
Molecular Weight:
232.21
MDL Number:
MOL File:
1401162-80-8.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:45

Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate Properties

storage temp. Sealed in dry,Room Temperature

Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate price More Price(20)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
aablocks AA001BYC Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate 98% 1401162-80-8 100mg $67 2026-05-28 Buy
aablocks AA001BYC Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate 98% 1401162-80-8 250mg $110 2026-05-28 Buy
aablocks AA001BYC Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate 98% 1401162-80-8 1g $303 2026-05-28 Buy
ACHEMBLOCK AD240146 methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate 95% 1401162-80-8 250MG $170 2026-05-27 Buy
ACHEMBLOCK AD240146 methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate 95% 1401162-80-8 1G $465 2026-05-27 Buy
Product number Packaging Price Buy
AA001BYC 100mg $67 Buy
AA001BYC 250mg $110 Buy
AA001BYC 1g $303 Buy
AD240146 250MG $170 Buy
AD240146 1G $465 Buy

Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate Chemical Properties,Uses,Production

Synthesis

2-Chloro-4-(4-fluoro-phenyl)-pyrimidine

85979-59-5

Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate

1401162-80-8

General procedure for the synthesis of methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate from 2-chloro-4-(4-fluorophenyl)-pyrimidine: In a 50 mL pressure vial, a methanol (20 mL) solution of 2-chloro-4-(4-fluorophenyl)pyrimidine (1 g, 4.79 mmol) was mixed with PdCl2 (dppf) (0.070 g, 0.096 mmol) and triethylamine (1.336 mL, 9.59 mmol) were mixed. The mixture was pressurized with carbon monoxide (60 psi) and the reaction was stirred at 100 °C for 15 hours. Upon completion of the reaction, the mixture was partitioned between 300 mL of ethyl acetate and 300 mL of water, the organic phase was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. The residue was separated by chromatography on a Grace Reveleris 40 g silica gel column, using a hexane solution of 0-100% ethyl acetate (flow rate 30 mL/min) as eluent, to afford the title compound, methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate (1.428 g, 6.15 mmol, 64.1% yield), as a brown solid.MS (ESI+ ) m/z 233.0 (M + H)+; 1H NMR (300 MHz, DMSO-d6) δ 9.02 (d, J = 5.4 Hz, 1H), 8.34 (dd, J = 9.1, 5.5 Hz, 2H), 8.29 (d, J = 5.4 Hz, 1H), 7.43 (t, J = 8.9 Hz, 2H), 3.95 (s, 3H).

References

[1] Patent: US2012/245124, 2012, A1. Location in patent: Page/Page column 39-40

85979-59-5
1401162-80-8
Synthesis of Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate from 2-Chloro-4-(4-fluoro-phenyl)-pyrimidine

Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate Preparation Products And Raw materials

Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate Suppliers

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Methyl 4-(4-fluorophenyl)pyrimidine-2-carboxylate 2-Pyrimidinecarboxylic acid, 4-(4-fluorophenyl)-, methyl ester 1401162-80-8