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2,5-di(thiophen-2-yl)-1,3-thiazole is a heterocyclic chemical compound that features a thiazole ring fused with two thiophene groups at the 2 and 5 positions. This unique structure, which includes both nitrogen and sulfur atoms in the thiazole ring and sulfur in the thiophene groups, endows the compound with distinctive electronic and optical properties. These characteristics make it a promising candidate for applications in the fields of organic electronics and material science.

54987-01-8

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54987-01-8 Usage

Uses

Used in Organic Electronics:
2,5-di(thiophen-2-yl)-1,3-thiazole is used as a component in organic semiconductors for its potential to enhance electronic properties. The presence of thiophene groups is expected to contribute to improved charge transport and stability in electronic devices.
Used in Material Science:
In the field of material science, 2,5-di(thiophen-2-yl)-1,3-thiazole is utilized as a building block for designing new materials with tailored properties. Its incorporation into polymers or other materials can lead to advancements in areas such as sensing, energy storage, and light-emitting technologies.
Further research is necessary to fully explore and exploit the capabilities of 2,5-di(thiophen-2-yl)-1,3-thiazole, ensuring that its potential in various applications is realized and optimized for practical use.

Check Digit Verification of cas no

The CAS Registry Mumber 54987-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,8 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 54987-01:
(7*5)+(6*4)+(5*9)+(4*8)+(3*7)+(2*0)+(1*1)=158
158 % 10 = 8
So 54987-01-8 is a valid CAS Registry Number.

54987-01-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dithiophen-2-yl-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 2,5-di(thiophen-2-yl)-1,3-thiazole

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:54987-01-8 SDS

54987-01-8Downstream Products

54987-01-8Relevant articles and documents

Design, synthesis and biological evaluation of novel N-(4-([2,2′:5′,2″-Terthiophen]-5-yl)-2-methylbut-3-yn-2-yl) benzamide derivatives

Zhu, Youquan,Zhang, Haili,Wang, Danyang,Li, Lei,Xu, Han,Li, Huabin,Ma, Yuan

, p. 268 - 276 (2015/03/04)

On the basis of the principle of combination of active groups, a series of novel N-(4-([2,2′:5′,2″-terthiophen]- 5-yl)-2-methylbut-3-yn-2-yl) benzamide derivatives were designed, synthesized and systematically evaluated for their antiviral activity agains

CONVENIENT SYNTHESIS OF VARIOUS TERHETEROCYCLIC COMPOUNDS BY Pd(O)-CATALYZED COUPLING REACTIONS

Gronowitz, Salo,Peters, Dan

, p. 645 - 658 (2007/10/02)

Various terheterocyclic compounds containing thiophene, furan, selenophene, pyridine and thiazole rings have been obtained by the Pd(PPh3)4-catalyzed coupling of dihalo-substituted heterocyclic compounds with heterocyclic boronic acids, using sodium bicar

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