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23767-44-4

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23767-44-4 Usage

Type of compound

Oxadiazole derivative
It belongs to a class of heterocyclic compounds with a five-membered ring containing two nitrogen atoms and one oxygen atom.

Functional groups

Methylthio and trimethoxyphenyl
The compound has a methylthio (-SCH3) group and a trimethoxyphenyl group (-C6H2(OCH3)3) attached to the oxadiazole ring.

Pharmacological properties

Anti-inflammatory, antioxidant, and anticancer activities
The compound has shown potential in treating various diseases due to its ability to reduce inflammation, neutralize harmful molecules, and inhibit cancer cell growth.

Potential applications

Drug development and materials science
It is being studied for its potential use in developing new drugs to treat diseases and in the development of new organic semiconductors and optoelectronic materials.

Structure

Planar and rigid
The oxadiazole ring is known for its planar and rigid structure, which can contribute to the compound's stability and biological activity.

Solubility

Likely soluble in organic solvents
Due to its nonpolar nature, the compound is expected to be soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO).

Stability

Relatively stable under normal conditions
The compound is expected to be stable under normal conditions, such as room temperature and atmospheric pressure, without undergoing significant degradation or transformation.

Synthesis

Can be synthesized through various chemical reactions
The compound can be synthesized through a series of chemical reactions, involving the formation of the oxadiazole ring and the attachment of the methylthio and trimethoxyphenyl groups.

Safety and handling

Should be handled with care due to potential biological activities
As with any chemical compound, especially one with potential pharmacological properties, it is essential to handle 1,3,4-Oxadiazole, 2-(methylthio)-5-(3,4,5-trimethoxyphenyl)with care, following proper safety protocols and guidelines.

Check Digit Verification of cas no

The CAS Registry Mumber 23767-44-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,6 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23767-44:
(7*2)+(6*3)+(5*7)+(4*6)+(3*7)+(2*4)+(1*4)=124
124 % 10 = 4
So 23767-44-4 is a valid CAS Registry Number.

23767-44-4SDS

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 2-methylthio-5-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names 5-(3,4,5-Trimethoxy-phenyl)-2-methylmercapto-1,3,4-oxadiazol

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:23767-44-4 SDS

23767-44-4Relevant articles and documents

Synthesis and antifungal activities of 5-(3,4,5-trimethoxyphenyl)-2-sulfonyl-1,3,4-thiadiazole and 5-(3,4,5-trimethoxyphenyl)-2-sulfonyl-1,3,4-oxadiazole derivatives

Chen, Cai-Jun,Song, Bao-An,Yang, Song,Xu, Guang-Fang,Bhadury, Pinaki S.,Jin, Lin-Hong,Hu, De-Yu,Li, Qian-Zhu,Liu, Fang,Xue, Wei,Lu, Ping,Chen, Zhuo

, p. 3981 - 3989 (2008/02/13)

Starting from the key intermediate 5-(3,4,5-trimethoxyphenyl)-1,3,4-thiadiazole-2-thiol (4) or the oxadiazole analogue (5), the title compounds 9 and 10 are synthesized by a two-step process. Thioetherification reaction of 4 or 5 with an organic halide ca

Synthesis and pharmacological activity of some 2(alkylaminoalkyl)mercapto 5 aryl 1,3,4 oxadiazoles

Mazzone,Bonina,Arrigo Reina

, p. 414 - 429 (2007/10/05)

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