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4-(2-METHYL-3-INDOLYL)PIPERIDINE is a chemical compound that features a piperidine ring fused with a 2-methyl-3-indolyl group at the 4-position. It is a derivative of both piperidine, a heterocyclic amine, and indole, a bicyclic aromatic compound. 4-(2-METHYL-3-INDOLYL)PIPERIDINE holds potential biological activities and is of interest in the field of pharmacology for its possible applications in drug discovery and development, serving as a building block for the synthesis of new pharmaceutical compounds. Further research is necessary to explore its full potential and properties.

65347-61-7

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65347-61-7 Usage

Uses

Used in Pharmaceutical Research:
4-(2-METHYL-3-INDOLYL)PIPERIDINE is used as a research compound for its potential pharmacological properties, which may contribute to the development of novel drugs.
Used in Drug Discovery and Development:
4-(2-METHYL-3-INDOLYL)PIPERIDINE is used as a building block in the synthesis of new pharmaceutical compounds, potentially leading to the creation of innovative medications.
Used in Chemical Synthesis:
In the chemical industry, 4-(2-METHYL-3-INDOLYL)PIPERIDINE may be utilized as an intermediate in the synthesis of complex organic molecules, given its unique structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 65347-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,4 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65347-61:
(7*6)+(6*5)+(5*3)+(4*4)+(3*7)+(2*6)+(1*1)=137
137 % 10 = 7
So 65347-61-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H18N2/c1-10-14(11-6-8-15-9-7-11)12-4-2-3-5-13(12)16-10/h2-5,11,15-16H,6-9H2,1H3

65347-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-3-piperidin-4-yl-1H-indole

1.2 Other means of identification

Product number -
Other names 2-methyl-3-piperidin-4-yl-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:65347-61-7 SDS

65347-61-7Upstream product

65347-61-7Relevant academic research and scientific papers

INDOLE DERIVATIVES USEFUL AS HISTAMINE H3 ANTAGONISTS

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Page 22, (2010/02/06)

Disclosed are novel compounds of the formula I wherein M1 is CH or N and M2 is C(R3) or N; R1 is optionally substituted indolyl or an aza derivative thereof; R2 is optionally substituted aryl or heteroaryl; and the remaining variables are as defined in the specification. Also disclosed are pharmaceutical compositions comprising the compounds of formula I. Also disclosed are methods of treating various diseases or conditions, such as, for example, allergy, allergy-induced airway responses, and congestion (e.g., nasal congestion) using the compounds of Formula I. Also disclosed are methods of treating various diseases or conditions, such as, for example, allergy, allergy-induced airway responses, and congestion (e.g., nasal congestion) using the compounds of formula I in combination with a H1 receptor antagonist.

Novel 1,4-benzodioxanes

-

, (2008/06/13)

Novel 1,4-benzodioxanes of the formula STR1 wherein R' is selected from the group consisting of hydrogen, alkoxy of 1 to 5 carbon atoms, chlorine, bromine and fluorine, R1 and R2 are individually selected from the group consisting of hydrogen and alkyl of 1 to 5 carbon atoms and Y and Z are hydrogen or together form a double bond in the form of their racemic mixtures or optically active isomers and their non-toxic, pharmaceutically acceptable acid addition salts having antihypertensive activity and a novel process and novel intermediates for their preparation.

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