製品名:1-benzyl-2-methylpiperidin-4-one

IUPAC Name:1-benzyl-2-methylpiperidin-4-one

CAS番号:203661-73-8
分子式:C13H17NO
純度:95%+
カタログ番号:CM107478
分子量:203.29

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製品詳細

CAS番号:203661-73-8
分子式:C13H17NO
融点:-
SMILESコード:O=C1CC(C)N(CC2=CC=CC=C2)CC1
密度:
カタログ番号:CM107478
分子量:203.29
沸点:
MDL番号:MFCD00480711
保管方法:

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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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.

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Product Other Information

Product Overview 1-benzyl-2-methylpiperidin-4-one, also known as BMPA, is a heterocyclic organic compound with a wide range of applications in pharmaceuticals, agrochemicals, and other industrial products. It is a versatile and widely used building block in organic synthesis due to its unique structure and properties. BMPA is a compound consisting of a benzyl group, a methyl group, and a piperidine ring. BMPA is a colorless liquid at room temperature and has a boiling point of 190°C.
Synthesis and Application 1-benzyl-2-methylpiperidin-4-one is typically synthesized through a condensation reaction between piperidine and benzaldehyde. The reaction is catalyzed by an acid, such as sulfuric acid, and yields 1-benzyl-2-methylpiperidin-4-one as a solid. The yields of the reaction can be improved by increasing the reaction temperature and reaction time. Additionally, 1-benzyl-2-methylpiperidin-4-one can also be synthesized through a condensation reaction between piperidine and dimethyl acetal. 1-benzyl-2-methylpiperidin-4-one has a variety of applications in scientific research. It is used as a starting material for the synthesis of other compounds, such as amino acids, peptides, and heterocyclic compounds. 1-benzyl-2-methylpiperidin-4-one is also used as a ligand in coordination chemistry, and as a reagent for the synthesis of organic compounds. Additionally, 1-benzyl-2-methylpiperidin-4-one is used as a catalyst in organic reactions, such as the Wittig reaction and the Biginelli reaction.
Future Directions The potential applications of 1-benzyl-2-methylpiperidin-4-one are vast and varied, and there are many opportunities for further research. For example, 1-benzyl-2-methylpiperidin-4-one could be studied for its potential applications in drug delivery systems, as a ligand in coordination chemistry, or as a catalyst in organic reactions. Additionally, 1-benzyl-2-methylpiperidin-4-one could be studied for its potential applications in materials science, such as in the synthesis of polymers and nanomaterials. Finally, 1-benzyl-2-methylpiperidin-4-one could be studied for its potential applications in agriculture, such as as a fungicide or pesticide.