3-Methyl-2-pyrazolin-5-one, 98+%, Thermo Scientific Chemicals

CAS: 108-26-9 | C4H6N2O | 98.105 g/mol

Catalog Number	Quantity
ALFA10253.18	50 g

Catalog number ALFA10253.18

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Chemical Identifiers

CAS7447-41-8

IUPAC Namelithium(1+) chloride

Molecular FormulaClLi

InChI KeyKWGKDLIKAYFUFQ-UHFFFAOYSA-M

SMILES[Li+].[Cl-]

Specifications

Assay (unspecified)99% min

3-Methyl-2-pyrazolin-5-one is used in the preparation of spirocyclic [indole-3,4'-pyrano[2,3-c]pyrazole] by reacting with isatins and malonitrile in the presence of sodium bromide as electrolyte.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Methyl-2-pyrazolin-5-one is used in the preparation of spirocyclic [indole-3,4′-pyrano[2,3-c]pyrazole] by reacting with isatins and malonitrile in the presence of sodium bromide as electrolyte.

Solubility
Slightly soluble in ethanol.

Notes
Incompatible with oxidizing agents.

RUO – Research Use Only

General References:

Vereshchagin, A. N.; Elinson, M. N.; Dorofeeva, E. O.; Nasybullin, R. F.; Bushmarinov, I. S.; Goloveshkin, A. S.; Egorov, M. P. Electrocatalytic cyclization of 3-(5-hydroxy-3-methylpyrazol-4-yl)-3-arylpropionitriles: ‘one-pot’ simple fast and efficient way to substituted spirocyclopropylpyrazolones. Electrochim. Acta 2015, 165, 116-121.
Wang, H. X.; Wu, L. L.; Wang, Y. M.; Zhou, Z. H. Organocatalyzed asymmetric tandem Michael-cyclization reaction of 4-benzylidene-3-methylpyrazol-5-ones and malononitrile: stereocontrolled construction of pyrano[2,3-c]pyrazole scaffold. RSC Adv. 2015, 5 (53), 42836-42842.