cas 41927-50-8|| where to buy 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one

Product Name:2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one

IUPAC Name:1-methyl-3-phenyl-4,5-dihydro-1H-pyrazol-5-one

: CAS：41927-50-8; Molecular Formula：C10H10N2O; Purity：95%

: Catalog Number：CM122942; Molecular Weight：174.2

Packing Unit	Available Stock	Price($)
CM122942-250mg	in stock	ȡǶȐ
CM122942-1g	in stock	ŵưũ

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Product Details

: CAS NO:41927-50-8; Molecular Formula:C10H10N2O; Melting Point:-; Smiles Code:O=C1CC(C2=CC=CC=C2)=NN1C; Density:

: Catalog Number:CM122942; Molecular Weight:174.2; Boiling Point:333.7°C at 760 mmHg; MDL No:MFCD00957095; Storage:Store at 2-8°C.

Category Infos

: Pyrazolines; Pyrazoline is a heterocyclic chemical compound with the molecular formula C3H6N2. Pyrazolines are well-known and important nitrogen-containing five-membered ring heterocyclic compounds. Pyrazoline derivatives have numerous prominent pharmacological effects, such as antimicrobial, anti-inflammatory, analgesic, antidepressant and anticancer.

Column Infos

: Pyrazoles; Pyrazoles are organic compounds of the general formula C3H3N2H. It is a five-membered heterocycle consisting of three carbon atoms and two adjacent nitrogen atoms. As an H-bond-donating heterocycle, pyrazole has been used as a more lipophilic and metabolically more stable bioisomer of phenol. Pyrazoles have attracted more and more attention due to their broad spectrum of action and strong efficacy.

: Benzenes; Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Product Other Information

Product Overview	2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one is a heterocyclic compound that has been widely studied in the laboratory due to its potential applications in the fields of medicinal chemistry, organic synthesis, and biochemistry. 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one is a five-membered ring structure, with a nitrogen atom at the center, and two methyl groups attached to the nitrogen atom.
Synthesis Method	The most common method is the condensation reaction of a 1,3-diketone with an amine. This is a two-step process, in which the 1,3-diketone is first reacted with an amine to form an imine, and then the imine is reacted with an acid to form the final product. Another method for synthesizing 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one is the reaction of a phenylhydrazine with a 1,3-diketone. This reaction is also a two-step process, in which the phenylhydrazine is first reacted with the 1,3-diketone to form an intermediate, and then the intermediate is reacted with an acid to form the final product.
Chemical Properties	It is a relatively stable molecule, which makes it easy to handle and store. In addition, 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one is relatively inexpensive and readily available, which makes it a cost-effective choice for laboratory experiments.
Synthesis and Application	In medicinal chemistry, 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one has been studied as a potential pharmaceutical agent. In organic synthesis, 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one has been used as a starting material in a variety of reactions, such as the condensation reaction with an amine and the reaction with a phenylhydrazine. In biochemistry, 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one has been studied for its potential use as a catalytic agent in enzymatic reactions.
Future Directions	The potential future directions for 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one include further research into its medicinal chemistry applications, such as the development of new pharmaceutical agents. In addition, further research into its biochemical and physiological effects could lead to the discovery of new therapeutic targets. Finally, further research into its organic synthesis applications could lead to the development of new methods for synthesizing 2-methyl-5-phenyl-2,4-dihydro-3H-pyrazol-3-one and other related compounds.