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3-(2-(4-(3-(trifluoromethyl)phenyl)-1-piperazinyl)ethyl)oxazolo(4,5-b)pyridin-2(3H)-one is a complex organic chemical compound with the molecular formula C21H21F3N4O2. It is a derivative of piperazine and belongs to the oxazolo(4,5-b)pyridin-2(3H)-one class of compounds. 3-(2-(4-(3-(trifluoromethyl)phenyl)-1-piperazinyl)ethyl)oxazolo(4,5-b)pyridin-2(3H)-one is of significant interest in the field of medicinal chemistry due to its potential pharmacological properties, particularly as an antagonist for specific receptors in the central nervous system. The presence of a trifluoromethyl group and a piperazine moiety are key structural features that enhance its biological activity, making it a promising candidate for further research and development in therapeutic applications.

134336-98-4

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134336-98-4 Usage

Uses

Used in Pharmaceutical Industry:
3-(2-(4-(3-(trifluoromethyl)phenyl)-1-piperazinyl)ethyl)oxazolo(4,5-b)pyridin-2(3H)-one is used as a potential therapeutic agent for the development of medications targeting the central nervous system. Its unique structure allows it to act as a receptor antagonist, which can be beneficial in treating various neurological and psychiatric disorders by modulating the activity of specific receptors.
Used in Research and Development:
In the field of medicinal chemistry, 3-(2-(4-(3-(trifluoromethyl)phenyl)-1-piperazinyl)ethyl)oxazolo(4,5-b)pyridin-2(3H)-one serves as a valuable research tool for understanding the interactions between molecules and their target receptors. It aids scientists in the discovery of new drugs and the optimization of existing ones by providing insights into the structure-activity relationships of receptor antagonists.
Used in Drug Design and Optimization:
3-(2-(4-(3-(trifluoromethyl)phenyl)-1-piperazinyl)ethyl)oxazolo(4,5-b)pyridin-2(3H)-one is utilized in the design and optimization of new drugs with improved efficacy, selectivity, and safety profiles. Its unique structural features can be modified to create a range of analogs with varying pharmacological properties, allowing researchers to fine-tune the compound's activity and minimize potential side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 134336-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,3,3 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134336-98:
(8*1)+(7*3)+(6*4)+(5*3)+(4*3)+(3*6)+(2*9)+(1*8)=124
124 % 10 = 4
So 134336-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C19H19F3N4O2/c20-19(21,22)14-3-1-4-15(13-14)25-10-7-24(8-11-25)9-12-26-17-16(28-18(26)27)5-2-6-23-17/h1-6,13H,7-12H2

134336-98-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[2-[4-[3-(trifluoromethyl)phenyl]piperazin-1-yl]ethyl]-[1,3]oxazolo[4,5-b]pyridin-2-one

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:134336-98-4 SDS

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