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1,3,4-Oxadiazole, 2,2',2''-(1,3,5-benzenetriyl)tris[5-phenylis a complex chemical compound that features an oxadiazole ring and a benzene ring. 1,3,4-Oxadiazole, 2,2',2''-(1,3,5-benzenetriyl)tris[5-phenylis recognized for its unique structural and electronic properties, which make it a valuable entity in the realm of organic chemistry. The presence of the oxadiazole ring endows the compound with strong electron-accepting characteristics, which are beneficial for the creation of organic semiconductors and electronic devices. The benzene ring further enhances the compound's aromatic nature and contributes to its overall stability and structure. 1,3,4-Oxadiazole, 2,2',2''-(1,3,5-benzenetriyl)tris[5-phenylholds promise for a range of applications in materials science and pharmaceuticals due to its versatile chemical properties.

148044-11-5

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148044-11-5 Usage

Uses

Used in Organic Semiconductors:
1,3,4-Oxadiazole, 2,2',2''-(1,3,5-benzenetriyl)tris[5-phenylis utilized as a key component in the development of organic semiconductors due to its strong electron-accepting properties. The oxadiazole ring plays a crucial role in enhancing the charge transport and stability of these semiconductors, making them suitable for applications in electronic devices such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs).
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 1,3,4-Oxadiazole, 2,2',2''-(1,3,5-benzenetriyl)tris[5-phenylis employed as a building block for the synthesis of various drug candidates. 1,3,4-Oxadiazole, 2,2',2''-(1,3,5-benzenetriyl)tris[5-phenyl-'s unique structure and electronic properties allow it to interact with biological targets, potentially leading to the development of new therapeutic agents with improved efficacy and selectivity.
Used in Materials Science:
1,3,4-Oxadiazole, 2,2',2''-(1,3,5-benzenetriyl)tris[5-phenyl-'s aromatic and structural properties make it a valuable material for use in the development of advanced materials with specific properties. For instance, it can be incorporated into polymers to improve their thermal stability, mechanical strength, or electrical conductivity, depending on the desired application.

Check Digit Verification of cas no

The CAS Registry Mumber 148044-11-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,0,4 and 4 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 148044-11:
(8*1)+(7*4)+(6*8)+(5*0)+(4*4)+(3*4)+(2*1)+(1*1)=115
115 % 10 = 5
So 148044-11-5 is a valid CAS Registry Number.

148044-11-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3,5-bis(5-phenyl-1,3,4-oxadiazol-2-yl)phenyl]-5-phenyl-1,3,4-oxadiazole

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

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More Details:148044-11-5 SDS

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