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2-piperidin-4-ylbenzonitrile is a chemical compound characterized by the presence of a piperidine ring fused to a benzene ring, featuring a nitrile functional group. This versatile molecule is recognized for its diverse pharmacological activities and serves as a crucial intermediate in the synthesis of a variety of pharmaceuticals.

304462-63-3

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304462-63-3 Usage

Uses

Used in Pharmaceutical Industry:
2-piperidin-4-ylbenzonitrile is utilized as a key intermediate in the synthesis of various drugs, leveraging its structural features to contribute to the development of new therapeutic agents.
Used in Antidepressant Development:
In the field of psychiatry, 2-piperidin-4-ylbenzonitrile is explored as a potential antidepressant, aiming to address the complex biochemical imbalances associated with mood disorders.
Used in Cancer Therapy:
2-piperidin-4-ylbenzonitrile is studied for its role as an enzyme inhibitor, targeting specific enzymes that play a role in the progression of cancer, thereby offering a potential therapeutic strategy against malignant diseases.
Used in Antipsychotic Medications:
2-piperidin-4-ylbenzonitrile is also investigated for its potential as an antipsychotic agent, suggesting its use in managing the symptoms of psychotic disorders by modulating neurotransmitter levels or receptor activity.
Used in Anticonvulsant Formulations:
2-piperidin-4-ylbenzonitrile is considered for its possible application in anticonvulsant medications, potentially helping to control seizures by influencing neuronal excitability.
Used in Organic Synthesis:
Beyond its direct pharmaceutical applications, 2-piperidin-4-ylbenzonitrile serves as a versatile building block in organic synthesis, enabling the creation of a wide range of chemical entities with potential applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 304462-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,4,4,6 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 304462-63:
(8*3)+(7*0)+(6*4)+(5*4)+(4*6)+(3*2)+(2*6)+(1*3)=113
113 % 10 = 3
So 304462-63-3 is a valid CAS Registry Number.

304462-63-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-piperidin-4-ylbenzonitrile

1.2 Other means of identification

Product number -
Other names 2-piperidin-4-ylbenzenecarbonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:304462-63-3 SDS

304462-63-3Downstream Products

304462-63-3Relevant academic research and scientific papers

PHENYL mTORC INHIBITORS AND USES THEREOF

-

, (2018/05/27)

The present invention provides compounds, compositions thereof, and methods of using the same.

(4-PHENYL-PIPERIDIN-1-YL)-[5-1H-PYRAZOL-4YL)-THIOPHEN-3-YL]-METHANONE COMPOUNDS AND THEIR USE

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, (2011/04/19)

The present invention pertains generally to the field of therapeutic compounds. More specifically the present invention pertains to certain (4-phenyl-piperidin-1-yl)- [5-(1 H-pyrazol-4-yl)-thiophen-3-yl]-methanone compounds that, inter alia, inhibit 11 β-hydroxysteroid dehydrogenase type 1 (11 β-HSD1 ). The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit 1 1 β-hydroxysteroid dehydrogenase type 1; to treat disorders that are ameliorated by the inhibition of 11 β-hydroxysteroid dehydrogenase type 1; to treat the metabolic syndrome, which includes disorders such as type 2 diabetes and obesity, and associated disorders including insulin resistance, hypertension, lipid disorders and cardiovascular disorders such as ischaemic (coronary) heart disease; to treat CNS disorders such as mild cognitive impairment and early dementia, including Alzheimer's disease; etc.

CYCLOALKANOPYRIDINE DERIVATIVE

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Page/Page column 68, (2010/11/24)

Provided are cycloalkanopyridine derivatives of formula [I]: [wherein the symbols are the same as those stated in the description]. The compounds act as a nociceptin receptor antagonist, and are useful as medicines for diseases associated with a nociceptin receptor, for example, as a reliever against tolerance to a narcotic analgesic; a reliever against dependence on or addiction to a narcotic analgesic; an analgesic enhancer; an antiobesitic or appetite suppressor; a treating or prophylactic agent for cognitive impairment and dementia/amnesia; an agent for treating developmental cognitive abnormality; a remedy for schizophrenia; an agent for treating neurodegenerative diseases; an anti-depressant or treating agent for affective disorder; a treating or prophylactic agent for diabetes insipidus; a treating or prophylactic agent for polyuria; or a remedy for hypotension.

An efficient synthesis of a highly functionalized 4-arylpiperidine

Boice, Geneviève N.,Savarin, Cécile G.,Murry, Jerry A.,Conrad, Karen,Matty, Louis,Corley, Edward G.,Smitrovich, Jacqueline H.,Hughes, Dave

, p. 11367 - 11374 (2007/10/03)

In this manuscript, an efficient synthesis of a functionalized 4-arylpiperidine is disclosed. Several synthetic approaches towards formation of the key aryl-piperidine sp3 carbon-carbon bond are discussed, including a scalable route to the piperidine via

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