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3515-49-9

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3515-49-9 Usage

Description

3-(4-Piperidylmethyl)-1H-indole, also known as PPI, is a heterocyclic chemical compound with the molecular formula C15H19N. It features a piperidylmethyl group attached to a 1H-indole ring, which endows it with unique pharmacological properties. This nitrogen-containing ring structure makes PPI a promising candidate in pharmaceutical research and drug development.

Uses

Used in Pharmaceutical Research and Drug Development:
3-(4-Piperidylmethyl)-1H-indole is used as a research compound for its potential as a serotonin receptor agonist, which is crucial for understanding its interaction with the nervous system and its implications for various therapeutic applications.
Used in Treatment of Neurological and Psychiatric Conditions:
In the field of neurology and psychiatry, 3-(4-Piperidylmethyl)-1H-indole is used as a potential treatment for conditions such as anxiety, depression, and schizophrenia. Its agonistic action on serotonin receptors may contribute to the modulation of mood and behavior, offering new avenues for managing these disorders.
Used in Parkinson's Disease Treatment:
3-(4-Piperidylmethyl)-1H-indole is being investigated for its potential use in the treatment of Parkinson's disease. Its role as a psychoactive substance suggests it may have the capacity to influence motor control and alleviate symptoms associated with this neurodegenerative condition.
Used in Psychopharmacology:
In psychopharmacology, 3-(4-Piperidylmethyl)-1H-indole is used as a substance of interest for its psychoactive properties. The ongoing research aims to determine its effects on cognitive function and emotional states, which could lead to the development of new therapeutic agents for various mental health conditions.
Further research is necessary to fully explore the potential therapeutic applications and pharmacological properties of 3-(4-Piperidylmethyl)-1H-indole, ensuring its safe and effective use in medical treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 3515-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3515-49:
(6*3)+(5*5)+(4*1)+(3*5)+(2*4)+(1*9)=79
79 % 10 = 9
So 3515-49-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2/c1-2-4-14-13(3-1)12(10-16-14)9-11-5-7-15-8-6-11/h1-4,10-11,15-16H,5-9H2

3515-49-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(piperidin-4-ylmethyl)-1H-indole

1.2 Other means of identification

Product number -
Other names 3-piperidin-4-ylmethyl-indole

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:3515-49-9 SDS

3515-49-9Downstream Products

3515-49-9Relevant articles and documents

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Gray

, p. 1453 (1958)

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3-(4-Piperidinylalkyl)indoles, Selective Inhibitors of Neuronal 5-Hydroxytryptamine Uptake

Gueremy, Claude,Audiau, Francois,Champseix, Alain,Uzan, Andre,Fur, Gerard Le,Rataud, Jean

, p. 1306 - 1310 (2007/10/02)

A series 3-(4-piperidinylalkyl)indoles was synthesized and tested as uptake inhibitors of biogenic amines.Some of these compounds are potent and very selective in blocking the 5-hydroxytryptamine (5-HT) uptake, as evidenced by biochemical data and behavioral tests.A discussion on structure-activity relationships is given.The most interesting member of the series, indalpine, 3-indole (1), was selected for clinical studies.

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