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25016-12-0

25016-12-0 Structure

25016-12-0 Structure
IdentificationBack Directory
[Name]

1,3-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE
[CAS]

25016-12-0
[Synonyms]

AKOS B000370
AKOS PAO-0261
TIMTEC-BB SBB000017
ART-CHEM-BB B000370
1,3-Dimethyl-4-formylpyrazole
1,3-dimethylpyrazole-4-carbaldehyde
1,3-Dimethylpyrazole-4-carboxaldehyde
3-diMethyl-1H-pyrazole-4-carbaldehyde
1,3-Dimethyl-1H-pyrazol-4-carbaldehyde
1,3-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE
1,3-DiMethyl-1H-pyrazole-4-carboxaldehyde
1H-Pyrazole-4-carboxaldehyde, 1,3-diMethyl-
1,3-dimethyl-1H-pyrazole-4-carbaldehyde(SALTDATA: FREE)
[Molecular Formula]

C6H8N2O
[MDL Number]

MFCD00159635
[MOL File]

25016-12-0.mol
[Molecular Weight]

124.14
Chemical PropertiesBack Directory
[Melting point ]

50℃
[Boiling point ]

98-100℃ (760 Torr)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C6H8N2O/c1-5-6(4-9)3-8(2)7-5/h3-4H,1-2H3
[InChIKey]

IGJREDVLGVEPFI-UHFFFAOYSA-N
[SMILES]

N1(C)C=C(C=O)C(C)=N1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H332-H312-H315-H319-H335-H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P280-P302+P352-P312-P322-P363-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

Xi
[HazardClass ]

IRRITANT
[HS Code ]

2933199090
Hazard InformationBack Directory
[Uses]

1,3-Dimethyl-1H-pyrazole-4-carbaldehyde is used in preparation of the inhibitors of SARM1 for the treatment or preventing of axonal degeneration.
[Synthesis]

ACETONEMETHYLHYDRAZONE

5771-02-8

N,N-Dimethylformamide

68-12-2

1H-Pyrazole-4-carboxaldehyde, 1,3-dimethyl-, 2-formyl-2-methylhydrazone

1353569-58-0

1,3-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE

25016-12-0

GENERAL PROCEDURE: Phosphorus oxychloride (POCl3, 0.1 mol) was slowly added dropwise to N,N-dimethylformamide (DMF, 20 mL) at 0°C. The mixture was cooled to -20°C and N-alkylhydrazone (0.05 mol) was added dropwise to DMF (10 mL) at that temperature. After 1 hour of reaction, the mixture was cooled to -20 °C and a solution of N-alkylhydrazone (0.05 mol) in DMF (10 mL) was slowly added dropwise at this temperature. The reaction was kept at -20 °C with stirring for 3 h. The temperature was then increased to 80 °C with continued stirring for 2 h. The reaction was then carried out at -20 °C with stirring. After completion of the reaction, the mixture was cooled to room temperature and carefully poured into ice (100 g). The mixture was adjusted to alkaline (pH=9-10) with 30% aqueous sodium hydroxide solution. The product was extracted with chloroform (CHCl3, 3 x 200 mL). The organic phases were combined and dried over anhydrous sodium sulfate (Na2SO4). The solvent was removed by concentration under reduced pressure and the residue was purified by vacuum distillation.

[References]

[1] Chemistry of Heterocyclic Compounds, 2011, vol. 47, # 8, p. 1048 - 1049
[2] Tetrahedron Letters, 2014, vol. 55, # 14, p. 2187 - 2189
[3] Chemistry of Heterocyclic Compounds, 2011, vol. 47, # 8, p. 1048 - 1049
Spectrum DetailBack Directory
[Spectrum Detail]

1,3-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE(25016-12-0)1HNMR
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