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1,3,4-Oxadiazol-2(3H)-one, 3-phenyl-, also known as 3-phenyl-1,2,4-oxadiazole or 3-phenyloxadiazole, is a heterocyclic compound with the molecular formula C7H5N2O2. It is a colorless crystalline solid that is soluble in organic solvents such as ethanol, acetone, and dichloromethane. This chemical is widely used in various applications, including as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. It is also employed as a ligand in coordination chemistry and as a reagent in organic synthesis. Due to its stability and versatility, 3-phenyl-1,2,4-oxadiazole is an important intermediate in the development of new compounds with potential applications in various industries.

7205-07-4

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7205-07-4 Usage

Type of compound

Heterocyclic compound

Structure

Contains an oxadiazole ring fused with a phenyl group

Applications

a. Building block in the synthesis of pharmaceutical compounds
b. Development of new drugs

Biological activities

a. Anti-inflammatory
b. Analgesic
c. Anti-cancer

Potential uses

a. Pesticide
b. Herbicide

Versatility

Highlighted by its potential applications in various fields

Pharmacological properties

Diverse, making it a valuable component in drug discovery and development

Research and development

Promising candidate for further research and development due to its unique structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 7205-07-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7205-07:
(6*7)+(5*2)+(4*0)+(3*5)+(2*0)+(1*7)=74
74 % 10 = 4
So 7205-07-4 is a valid CAS Registry Number.

7205-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-3H-[1,3,4]oxadiazol-2-one

1.2 Other means of identification

Product number -
Other names 4-Phenyl-

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:7205-07-4 SDS

7205-07-4Relevant academic research and scientific papers

One-pot synthesis of 1,3,4-oxadiazol-2(3H)-ones with CO2 as a C1 synthon promoted by hypoiodite

Yang, Na,Yuan, Gaoqing

, p. 6639 - 6644 (2019/07/16)

A convenient and efficient route has been developed to synthesize 1,3,4-oxadiazol-2(3H)-ones from CO2, hydrazines and aryl or aliphatic aldehydes. Promoted by hypoiodite (IO-) generated in situ from KI and oxidant TBHP, the one-pot synthesis could proceed smoothly to afford the desired products in moderate to high yields. Mechanism studies revealed that nitrile imine was an important intermediate in this transformation. Notably, a commercial herbicide Oxadiazon could be successfully synthesized by this route.

A novel electrochemical conversion of CO2 with aryl hydrazines and paraformaldehyde into 1,3,4-oxadiazol-2(3H)-one derivatives in one step

Yang, Na,Lai, Qiang,Jiang, Huanfeng,Yuan, Gaoqing

, p. 109 - 112 (2016/09/28)

Using CO2 to replace phosgene or CO as the C1 synthon, we successfully achieved the one-pot electrochemical synthesis of 1,3,4-oxadiazol-2(3H)-one derivatives via a three-component coupling reaction of CO2 with aryl hydrazines and pa

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