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3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE, a benzoxazolone derivative with a molecular formula of C15H16N2O2, is a chemical compound that features a piperidine ring. It is recognized for its potential as a building block in the synthesis of pharmaceutical and agrochemical compounds. Additionally, this compound has garnered interest due to its possible biological activity, particularly as a serotonin receptor antagonist. 3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE's specific applications and uses are currently a subject of ongoing research and exploration within the realms of chemistry and pharmaceutical science.

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  • 215878-20-9 Structure
  • Basic information

    1. Product Name: 3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE
    2. Synonyms: 3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE;3-(piperidin-4-yl)benzo[d]oxazol-2(3H)-one;3-(4-piperidinyl)-2(3H)-Benzoxazolone;-1,3-benzoxazol-2(3H);3-(4-Piperidinyl)
    3. CAS NO:215878-20-9
    4. Molecular Formula: C12H14N2O2
    5. Molecular Weight: 218.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215878-20-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 355.8°C at 760 mmHg
    3. Flash Point: 169°C
    4. Appearance: /
    5. Density: 1.259g/cm3
    6. Vapor Pressure: 3.05E-05mmHg at 25°C
    7. Refractive Index: 1.596
    8. Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE(215878-20-9)
    12. EPA Substance Registry System: 3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE(215878-20-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 215878-20-9(Hazardous Substances Data)

215878-20-9 Usage

Uses

Used in Pharmaceutical Synthesis:
3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE is used as a chemical building block for the synthesis of various pharmaceutical compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE is utilized as a key intermediate in the creation of agrochemicals. Its incorporation can lead to the development of novel pesticides or other agricultural chemicals that may offer enhanced efficacy or selectivity.
Used in Biological Research:
3-(4-PIPERIDINYL)-1,3-BENZOXAZOL-2(3H)-ONE is employed as a research tool in biological studies, particularly for investigating its role as a serotonin receptor antagonist. This application aids in understanding its potential impact on biological systems and may contribute to the discovery of new therapeutic agents targeting the serotonin system.

Check Digit Verification of cas no

The CAS Registry Mumber 215878-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,8,7 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 215878-20:
(8*2)+(7*1)+(6*5)+(5*8)+(4*7)+(3*8)+(2*2)+(1*0)=149
149 % 10 = 9
So 215878-20-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H14N2O2/c15-12-14(9-5-7-13-8-6-9)10-3-1-2-4-11(10)16-12/h1-4,9,13H,5-8H2

215878-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-piperidin-4-yl-1,3-benzoxazol-2-one

1.2 Other means of identification

Product number -
Other names 3-piperidin-4-yl-3H-benzooxazol-2-one

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:215878-20-9 SDS

215878-20-9Relevant articles and documents

HETEROCYCLIC COMPOUND, APPLICATION THEREOF, AND COMPOSITION CONTAINING SAME

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, (2022/03/07)

A heterocyclic compound represented by formula XI, a pharmaceutically acceptable salt, a solvate, or a solvate of a pharmaceutically acceptable salt thereof, use thereof, and a composition containing the same. The compound is novel in structure and has good STAT5 inhibitory activity.

DIPHENYLBUTYPIPERIDINE AUTOPHAGY INDUCERS

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Page/Page column 7; 87-90, (2011/12/02)

Autophagy inducing compounds, methods of their preparation and use, and kits containg said compounds are disclosed herein.

Piperidine amides as 11β-hydroxysteroid dehydrogenase type 1 inhibitors

Flyrén, Katarina,Bergquist, Lars O.,Castro, Victor M.,Fotsch, Christopher,Johansson, Lars,St. Jean Jr., David J.,Sutin, Lori,Williams, Meredith

, p. 3421 - 3425 (2008/02/08)

A series of piperidine amide inhibitors of human 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) were identified via modifications of the HTS hit compound 1. The synthesis, in vitro biological evaluation, and structure-activity relationship of these co

Method for treating allergies using substituted pyrazoles

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, (2008/06/13)

A method for treating an allergic condition, including an atopic allergic condition, using substituted pyrazoles.

Design and synthesis of N-alkylated saccharins as selective α-1a adrenergic receptor antagonists

Nerenberg, Jennie B.,Erb, Jill M.,Thompson, Wayne J.,Lee, Hee-Yoon,Guare, James P.,Munson, Peter M.,Bergman, Jeffrey M.,Huff, Joel R.,Broten, Theodore P.,Chang, Raymond S. L.,Chen, Tsing B.,O'Malley, Stacey,Schorn, Terry W.,Scott, Ann L.

, p. 2467 - 2472 (2007/10/03)

Benign prostatic hyperplasia can be managed pharmacologically with α-1 adrenergic receptor antagonists. Agents that demonstrate selectivity for the α-la receptor subtype may offer advantages in clinical applications with respect to hypotensive side effect

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