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Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI)

Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) Suppliers list
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Products Intro: Product Name:2-Chloro-5-fluoro-4-methylpyrimidine
CAS:134000-96-7
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:2-Chloro-5-fluoro-4-methylpyrimidine
CAS:134000-96-7
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-33746
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CAS:134000-96-7
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CAS:134000-96-7
Purity:0.98 Package:1g; 5g; 10g; 25g; 100g
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Products Intro: Product Name:Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI)
CAS:134000-96-7
Purity:99.00% Package:1g;1.1USD Remarks:ISO 9001:2015 REACH Approved Manufacturer

Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) manufacturers

Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) Basic information
Product Name:Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI)
Synonyms:Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI);2-Chloro-5-fluoro-4-methylpyrimidine;PyriMidine, 2-chloro-5-fluoro-4-Methyl-;Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) ISO 9001:2015 REACH
CAS:134000-96-7
MF:C5H4ClFN2
MW:146.55
EINECS:
Product Categories:Fluorine series;PYRIMIDINE
Mol File:134000-96-7.mol
Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) Structure
Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) Chemical Properties
Boiling point 220℃
density 1.352
Fp 87℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka-2.05±0.29(Predicted)
AppearanceWhite to yellow Solid
Safety Information
HS Code 2933599590
MSDS Information
Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) Usage And Synthesis
Synthesis
Methylmagnesium Bromide

75-16-1

2,4-Dichloro-5-fluoropyrimidine

2927-71-1

Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI)

134000-96-7

Intermediate 55: Synthesis of 2-chloro-5-fluoro-4-methylpyrimidine. 2,4-Dichloro-5-fluoropyrimidine (1.02 g, 6.08 mmol) and Fe(acac)3 (215 mg, 0.61 mmol) were dissolved in a THF/NMP solvent mixture (38 mL/3 mL) and the mixture was cooled to 0 °C. A 3.0 M solution of Et2O of methylmagnesium bromide (3.04 mL, 9.12 mmol) was added slowly and dropwise. The reaction was completed after 30 min at 0 °C and quenched with saturated aqueous NH4Cl solution. Et2O was added for stratification and the aqueous layer was extracted several times with Et2O. The organic layers were combined, dried with Na2SO4, filtered and concentrated in vacuum. Purification by column chromatography (eluent: hexane to 10% EtOAc/hexane) afforded the target product 2-chloro-5-fluoro-4-methylpyrimidine as a waxy white solid (430 mg, 48% yield).1H NMR (400 MHz, CDCl3): δ 8.35 (s, 1H), 2.55 (d, J=2.5 Hz, 3H).

References[1] Journal of Medicinal Chemistry, 2014, vol. 57, # 8, p. 3263 - 3282
[2] Patent: WO2011/50200, 2011, A1. Location in patent: Page/Page column 84
[3] Patent: WO2011/50198, 2011, A1. Location in patent: Page/Page column 74
[4] Patent: WO2012/145581, 2012, A1. Location in patent: Page/Page column 74
[5] Patent: WO2015/89143, 2015, A1. Location in patent: Page/Page column 95
Pyrimidine, 2-chloro-5-fluoro-4-methyl- (9CI) Preparation Products And Raw materials
Raw materialsMethylmagnesium chloride-->Methylmagnesium Bromide-->2,4-Dichloro-5-fluoropyrimidine
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