Basic information Uses Synthesis Safety Supplier Related
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methyl 2-chloropyrimidine-4-carboxylate

Basic information Uses Synthesis Safety Supplier Related

methyl 2-chloropyrimidine-4-carboxylate Basic information

Product Name:
methyl 2-chloropyrimidine-4-carboxylate
Synonyms:
  • methyl 2-chloropyrimidine-4-carboxylate
  • 2-Chloro-4-(methoxycarbonyl)pyrimidine
  • 4-PyriMidinecarboxylic acid, 2-chloro-, Methyl ester
  • 4-PyriMidinecarboxylic ac...
  • 2-Chloro-pyriMidine-4-carboxylic acid Methyl ester
  • 2-Chloro-4-(methoxycarbonyl)pyrimidine, 2-Chloro-4-(methoxycarbonyl)-1,3-diazine
  • 2-Chloro-pyrimidin-4-carboxylic acid methyl ester
  • 2-chloro-4-Pyrimidinecarboxylic acid methyl ester
CAS:
149849-94-5
MF:
C6H5ClN2O2
MW:
172.57
EINECS:
687-723-0
Product Categories:
  • Heterocycle-Pyrimidine series
Mol File:
149849-94-5.mol
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methyl 2-chloropyrimidine-4-carboxylate Chemical Properties

Boiling point:
304.3±15.0 °C(Predicted)
Density 
1.372±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-3.78±0.20(Predicted)
form 
solid
Appearance
Off-white to light yellow Solid
InChI
InChI=1S/C6H5ClN2O2/c1-11-5(10)4-2-3-8-6(7)9-4/h2-3H,1H3
InChIKey
GGTNGWOGJHJQCL-UHFFFAOYSA-N
SMILES
C1(Cl)=NC=CC(C(OC)=O)=N1
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
36/37/39
WGK Germany 
3
HS Code 
29335990
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methyl 2-chloropyrimidine-4-carboxylate Usage And Synthesis

Uses

Methyl 2-chloropyrimidine-4-carboxylate is an organic ester, which can be used as an intermediate in pharmaceutical synthesis for experimental research and pharmaceutical synthesis.

Synthesis

Synthesis of methyl 2-chloropyrimidine-4-carboxylate: 2-chloropyrimidine-4-carboxylic acid (4.76 g, 30 mmol) was dissolved in dichloromethane (30 mL) and dimethylformamide (0.3 mL), to which was added Slowly add oxalyl chloride (5.72g, 45mmol) dropwise, stir at room temperature for 2 hours, Chemicalbook, after concentrating to an appropriate volume, add dropwise to anhydrous methanol (50mL) placed under ice bath conditions, after the dropwise addition, the reaction is transferred to The reaction was carried out at room temperature for 2 hours, and concentrated under reduced pressure to obtain (5.17 g, yield 100%).

References

[1] Patent: US2007/225271, 2007, A1. Location in patent: Page/Page column 33

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