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595567-05-8

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595567-05-8 Usage

Explanation

Different sources of media describe the Explanation of 595567-05-8 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. This compound belongs to a class of chemical compounds that contain an oxadiazole ring, which is a five-membered ring with two nitrogen atoms and one oxygen atom.
3. The core structure of the compound is a 1,3,4-oxadiazole ring, which is a type of oxadiazole ring with specific positions of the nitrogen and oxygen atoms.
4. The 4-fluorophenyl group is a phenyl ring (a six-membered ring with alternating single and double carbon-carbon bonds) with a fluorine atom attached to the fourth carbon atom.
5. Due to its biological and physical properties, this compound has potential uses in various industries, including the development of new drugs, agricultural chemicals, and advanced materials.
6. The compound has been found to exhibit a range of biological activities, which could make it useful in the development of new treatments for various diseases and conditions.
7. The specific arrangement of atoms and functional groups in the compound's structure makes it a promising candidate for the development of new drugs and materials with desirable properties.
8. Current research efforts are focused on understanding the compound's properties and potential applications in various fields, with the aim of maximizing its usefulness and impact.

Class

Oxadiazole compounds

Core structure

1,3,4-oxadiazole

Substituent

4-fluorophenyl group

Potential applications

Pharmaceuticals, agrochemicals, and materials science

Biological activities

Antimicrobial, anticancer, anti-inflammatory, and antiviral properties

Unique structure

Potential candidate for new drugs and materials

Ongoing research

Exploring full potential and applicability

Check Digit Verification of cas no

The CAS Registry Mumber 595567-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,5,5,6 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 595567-05:
(8*5)+(7*9)+(6*5)+(5*5)+(4*6)+(3*7)+(2*0)+(1*5)=208
208 % 10 = 8
So 595567-05-8 is a valid CAS Registry Number.

595567-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-fluorophenyl)-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names 2-(4-Fluoro-phenyl)-[1,3,4]oxadiazole

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:595567-05-8 SDS

595567-05-8Relevant articles and documents

[4u202f+u202f1] Cyclization of benzohydrazide and ClCF2COONa towards 1,3,4-oxadiazoles and 1,3,4-oxadiazoles-d5

Li, Xin,Mu, Shiqiang,Song, Qiuling,Wang, Ya

supporting information, (2021/09/20)

A facile synthesis of 1,3,4-oxadiazoles and 1,3,4-oxadiazoles-d5 via [4 + 1] cyclization of ClCF2COONa with non-amine compounds containing amino groups is developed. Of note, this is the first time that halofluorinated compounds are used as C1 synthon to construct deuterated nitrogen-heterocyclic compounds. The current protocol features simple operation, readily accessible raw materials, wide substrate scope and valuable products

TiCl4 mediated facile synthesis of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles

Zhang, Lin,Yu, Yu,Tang, Qiang,Yuan, Jianyong,Ran, Dongzhi,Tian, Binghua,Pan, Tao,Gan, Zongjie

, p. 423 - 431 (2019/12/27)

An efficient method for the synthesis of 2,5-disubstituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles has been developed. Various hydrazides or thionyl hydrazides readily react with DMA derivatives in the presence of TiCl4 as a catalyst to afford the desired products. This protocol provides a simple and economical procedure that affords the target products with good yields and wide substrate scope.

Method for constructing 2-(4-fluorophenyl)-1,3,4-oxadiazole by taking DMF as carbon source at one step

-

Paragraph 0016-0023, (2019/02/26)

The invention discloses a method for constructing 2-(4-fluorophenyl)-1,3,4-oxadiazole by taking DMF (N,N-dimethylformamide) as a carbon source at one step. The method comprises the following steps: taking p-fluorobenzhydrazide as a reaction raw material;

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