Basic information Safety Supplier Related

1,3-DIMETHYL-1H-PYRAZOLE-5-CARBALDEHYDE

Basic information Safety Supplier Related

1,3-DIMETHYL-1H-PYRAZOLE-5-CARBALDEHYDE Basic information

Product Name:
1,3-DIMETHYL-1H-PYRAZOLE-5-CARBALDEHYDE
Synonyms:
  • 1,3-DIMETHYLPYRAZOLE-5-CARBOXALDEHYDE
  • 1,3-DIMETHYL-1H-PYRAZOLE-5-CARBALDEHYDE
  • 1,3-DIMETHYL-1H-PYRAZOLE-5-CARBOXALDEHYDE
  • AKOS B015985
  • 2,5-DIMETHYL-2 H-PYRAZOLE-3-CARBALDEHYDE
  • ART-CHEM-BB B015985
  • 1,3-Dimethylpyrazole-5-carbaldehyde
  • 1,3-Dimethyl-1h-pyrazole-5-carbaldehyde, 90+%
CAS:
25016-09-5
MF:
C6H8N2O
MW:
124.14
Mol File:
25016-09-5.mol
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1,3-DIMETHYL-1H-PYRAZOLE-5-CARBALDEHYDE Chemical Properties

Melting point:
40-42°C
Boiling point:
80-83 °C(Press: 12 Torr)
Density 
1.11±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
1.03±0.10(Predicted)
form 
solid
Appearance
Colorless to light yellow Liquid
CAS DataBase Reference
25016-09-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39
HazardClass 
IRRITANT
HS Code 
29331990
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1,3-DIMETHYL-1H-PYRAZOLE-5-CARBALDEHYDE Usage And Synthesis

Chemical Properties

Colorless to light yellow liquid

Synthesis

57012-20-1

25016-09-5

Step 2: Preparation of 2,5-dimethyl-2H-pyrazole-3-carbaldehyde (15) A mixture of compound 14 (1,3-dimethyl-5-hydroxymethyl-1H-pyrazole, 3 g, 23.8 mmol) with pyridinium dichromate (13.4 g, 35.7 mmol) in dichloromethane (100 ml) was reacted for 16 hrs at 25°C under nitrogen protection with stirring. After completion of the reaction, the reaction mixture was filtered and the filtrate was collected. The filtrate was dried over anhydrous Na2SO4 and concentrated under reduced pressure to remove the solvent. The resulting crude product was purified by silica gel column chromatography to afford the target product 2,5-dimethyl-2H-pyrazole-3-carbaldehyde (15) as a 1 g brown solid in 34% yield. Product characterization data: 1H NMR (200 MHz, CDCl3): δ 9.8 (s, 1H), 6.6 (s, 1H), 4.1 (s, 3H), 2.3 (s, 3H). Mass spectrum (CI method, isobutane): 125 (M + 1, 100%). IR spectrum (KBr, cm-1): νmax 1688.

References

[1] Patent: US2006/128729, 2006, A1. Location in patent: Page/Page column 98
[2] Patent: WO2005/9941, 2005, A1. Location in patent: Page 45-46
[3] Patent: WO2009/101082, 2009, A1. Location in patent: Page/Page column 71

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