製品名: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番号:41927-50-8
分子式:C10H10N2O
純度:95%
カタログ番号:CM122942
分子量:174.2

包装単位 有効在庫 価格(USD) 数量
CM122942-250mg in stock ĜƏƩ
CM122942-1g in stock ǭǎŁ

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製品詳細

CAS番号:41927-50-8
分子式:C10H10N2O
融点:-
SMILESコード:O=C1CC(C2=CC=CC=C2)=NN1C
密度:
カタログ番号:CM122942
分子量:174.2
沸点:333.7°C at 760 mmHg
MDL番号:MFCD00957095
保管方法: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.