Nombre del producto:1-phenylpiperidine-4-carboxylic acid hydrochloride

IUPAC Name:1-phenylpiperidine-4-carboxylic acid hydrochloride

CAS:209005-67-4
Fórmula molecular:C12H16ClNO2
Pureza:95%
Número de catálogo:CM128036
Peso molecular:241.72

Unidad de embalaje Stock disponible Precio($) Cantidad
CM128036-250mg in stock ƴǎ
CM128036-1g in stock řijħ

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Detalles del producto

Núm. De CAS :209005-67-4
Fórmula molecular:C12H16ClNO2
Punto de fusión:-
Código de sonrisas:O=C(C1CCN(C2=CC=CC=C2)CC1)O.[H]Cl
Densidad:
Número de catálogo:CM128036
Peso molecular:241.72
Punto de ebullición:
Nº Mdl:
Almacenamiento:Store at room temperature.

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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Product Other Information

Product Overview 1-phenylpiperidine-4-carboxylic acid hydrochloride (1-PPCH) is a type of piperidine derivative that has found a wide range of applications in the scientific research and laboratory fields. It has been used in a number of biochemical and physiological experiments, as well as being a key component in the synthesis of several other compounds.
Synthesis and Application 1-phenylpiperidine-4-carboxylic acid hydrochloride is synthesized through a process known as acid-catalyzed condensation. This involves the reaction of an acid-catalyzed condensation of 1-phenylpiperidine-4-carboxylic acid and hydrochloric acid. The reaction is typically carried out in a non-aqueous solution of ethyl acetate or another organic solvent, such as acetonitrile or dimethyl sulfoxide, at a temperature of around 60°C. The reaction is usually complete within a few hours, and the product is then purified by recrystallization. 1-Phenylpiperidine-4-carboxylic acid hydrochloride has been used in a variety of scientific research applications. It has been used as a model compound for the study of the structure-activity relationships of piperidine derivatives. It has also been used as a starting material for the synthesis of other compounds, such as 2-methyl-1-phenylpiperidine-4-carboxylic acid and 2-methyl-1-phenylpiperidine-4-carboxylic acid hydrochloride. In addition, 1-phenylpiperidine-4-carboxylic acid hydrochloride has been used as a reagent in the synthesis of several pharmaceuticals and other compounds.
Future Directions 1-phenylpiperidine-4-carboxylic acid hydrochloride has a wide range of potential future applications in the scientific research and laboratory fields. One possible application is in the synthesis of other compounds, such as pharmaceuticals and other piperidine derivatives. Additionally, further research into the biochemical and physiological effects of 1-phenylpiperidine-4-carboxylic acid hydrochloride could lead to the development of new treatments for a variety of conditions, such as cognitive impairment and muscle weakness. Finally, 1-phenylpiperidine-4-carboxylic acid hydrochloride could be used as a tool to study the structure-activity relationships of other piperidine derivatives.