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4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine is a chemical compound characterized by a molecular formula of C9H16N4O. It features a piperidine ring that is substituted with a 5-methyl-1,3,4-oxadiazol-2-yl group, which contributes to its unique chemical and biological properties. 4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine is of interest in pharmaceutical research and development due to its potential as a drug candidate.

161609-79-6

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161609-79-6 Usage

Uses

Used in Pharmaceutical Research and Development:
4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine is used as a potential drug candidate for the treatment of various medical conditions. Its specific applications are still under investigation, but its unique structure and properties suggest it may have therapeutic potential in a range of areas.
Used in Structure-Activity Relationship Studies:
In the field of medicinal chemistry, 4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine is used as a valuable tool for studying the structure-activity relationships of related compounds. This helps researchers understand how variations in chemical structure can influence biological activity, which is crucial for the development of new and improved pharmaceuticals.
Used in Drug Design and Optimization:
4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine's structure and properties make it a useful starting point for drug design and optimization processes. By exploring modifications to the 4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine scaffold, researchers can potentially identify new compounds with enhanced therapeutic effects and improved pharmacokinetic profiles.
Used in the Development of Novel Therapeutic Agents:
Given its potential as a drug candidate, 4-(5-methyl-1,3,4-oxadiazol-2-yl)piperidine may be employed in the development of novel therapeutic agents targeting a variety of diseases and conditions. Further research is necessary to determine its exact applications and to optimize its properties for maximum therapeutic benefit.

Check Digit Verification of cas no

The CAS Registry Mumber 161609-79-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,6,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 161609-79:
(8*1)+(7*6)+(6*1)+(5*6)+(4*0)+(3*9)+(2*7)+(1*9)=136
136 % 10 = 6
So 161609-79-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H13N3O/c1-6-10-11-8(12-6)7-2-4-9-5-3-7/h7,9H,2-5H2,1H3

161609-79-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-piperidin-4-yl-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names F2184-0013

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:161609-79-6 SDS

161609-79-6Upstream product

161609-79-6Downstream Products

161609-79-6Relevant academic research and scientific papers

Aryl substituted heterocycles

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, (2008/06/13)

The present invention concerns the novel use of aryl substituted heterocycles of formula I, set out below, which antagonize the pharmacological actions of one of ent endogenous neuropeptide tachykinins an the neurokinin 2 (NK2) receptor making them useful whenever such antagonism is desired, such as in the treatment of asthma and related conditions. The invention also provides pharmaceutical compositions containing the aryl substituted heterocycles for use in such treatment. Certain novel aryl substituted heterocycles of formula I and novel intermediates for their manufacture are also provided. STR1

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