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3,4-PYRIDINEDICARBOXIMIDE

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3,4-PYRIDINEDICARBOXIMIDE Basic information

Product Name:
3,4-PYRIDINEDICARBOXIMIDE
Synonyms:
  • 3,4-PYRIDINEDICARBOXIMIDE
  • 1H-PYRROLO[3,4-C]PYRIDINE-1,3(2H)-DIONE
  • 2,3-DIHYDRO-1H-PYRROLO[3,4-C]PYRIDINE-1,3-DIONE
  • CINCHOMERONIMIDE
  • BUTTPARK 48\06-51
  • 3,4-Pyridinedicarboximide ,97%
  • 2H-Pyrrolo[3,4-c]pyridine-1,3-dione
  • 3,4-Pyridinedicarbimide
CAS:
4664-01-1
MF:
C7H4N2O2
MW:
148.12
EINECS:
628-277-9
Mol File:
4664-01-1.mol
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3,4-PYRIDINEDICARBOXIMIDE Chemical Properties

Melting point:
232-235 °C(lit.)
Boiling point:
268.69°C (rough estimate)
Density 
1.4015 (rough estimate)
refractive index 
1.5300 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
7.80±0.20(Predicted)
form 
Crystalline Powder
color 
White to tan
InChI
InChI=1S/C7H4N2O2/c10-6-4-1-2-8-3-5(4)7(11)9-6/h1-3H,(H,9,10,11)
InChIKey
SJSABZBUTDSWMJ-UHFFFAOYSA-N
SMILES
C1=NC=CC2C(=O)NC(=O)C1=2
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
RTECS 
US7966000
HazardClass 
IRRITANT
HS Code 
29333990

MSDS

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3,4-PYRIDINEDICARBOXIMIDE Usage And Synthesis

Chemical Properties

White to light brown powder

Synthesis

490-11-9

4664-01-1

The general procedure for the synthesis of 3,4-pyridinedicarboxylic acid as a raw material for the synthesis of 3,4-pyridinedicarboximides was as follows: firstly, sublimated 3,4-pyridinedicarboxylic acid (50 g, 300 mmol) was suspended in acetic anhydride (123.5 g, 1,200 mmol), and heated to reflux (140-150 °C) until the solid was completely dissolved and the mixture presented homogeneous state. Subsequently, the reaction mixture was cooled and concentrated under vacuum. Next, acetamide (50 g, 846 mmol) was added to the concentrate and the mixture was heated and reacted at 140 °C for 3 hours. After completion of the reaction, the mixture was cooled to room temperature. The solid residue formed during cooling was pulverized, ground with 100 ml of water, filtered and washed with additional water. Finally, the resulting solid was dried in a desiccator to afford 3,4-pyridinedicarboximide (42.26 g, 95.1% yield), which met the purity requirements for use without further purification. The product was analyzed by LC-MS showing a m/z (ESP) of 149 [M + H]+ and a retention time (R/T) of 0.44 min.

References

[1] Patent: US2006/199804, 2006, A1. Location in patent: Page/Page column 29
[2] Acta Chimica Hungarica, 1983, vol. 112, # 4, p. 487 - 500

3,4-PYRIDINEDICARBOXIMIDE Preparation Products And Raw materials

Raw materials

3,4-PYRIDINEDICARBOXIMIDESupplier

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