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6641-96-9

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6641-96-9 Usage

Molecular structure

A complex structure consisting of a thiazole ring fused with another thiazole ring and two phenyl groups attached to the 2 and 5 positions of the thiazole rings.

Type of compound

A chemical compound belonging to the class of thiazoles.

Unique value

Its unique structure makes it a valuable target for chemical synthesis and research into its properties and potential uses.

Position of phenyl groups

The two phenyl groups are attached to the 2 and 5 positions of the thiazole rings, which may influence its electronic and optical properties.

Fusion of rings

The fusion of the two thiazole rings in the structure contributes to the compound's stability and potential applications in electronic materials.

Electronic and optical properties

The specific electronic and optical properties of 2,5-diphenyl[1,3]thiazolo[5,4-d][1,3]thiazole have not been provided, but they are likely to be unique and of interest for research and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6641-96-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6641-96:
(6*6)+(5*6)+(4*4)+(3*1)+(2*9)+(1*6)=109
109 % 10 = 9
So 6641-96-9 is a valid CAS Registry Number.

6641-96-9SDS

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 2,5-diphenyl-[1,3]thiazolo[5,4-d][1,3]thiazole

1.2 Other means of identification

Product number -
Other names thiazolo[5,4-d]thiazole,2,5-diphenyl

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:6641-96-9 SDS

6641-96-9Relevant articles and documents

Synthesis and spectroscopic-voltammetric behaviors of silver(I) 2,5-diphenylthiazolo[5,4-d]thiazole

Olgun, U?ursoy,Gülfen, Mustafa

, p. 1004 - 1009 (2013)

In the present work, 2,5-diphenylthiazolo[5,4-d]thiazole (DTT) and silver(I) 2,5-diphenylthiazolo[5,4-d]thiazole complex(Ag2DTT) were synthesized, and then their spectroscopic and voltammetric behaviors were investigated. The DTT was obtained b

Exploration of Thiazolo[5,4-d]thiazole Linkages in Conjugated Porous Organic Polymers for Chemoselective Molecular Sieving

Biswal, Bishnu P.,Becker, Daniel,Chandrasekhar, Naisa,Seenath, Jensheer Shamsudeen,Paasch, Silvia,Machill, Susanne,Hennersdorf, Felix,Brunner, Eike,Weigand, Jan J.,Berger, Reinhard,Feng, Xinliang

supporting information, p. 10868 - 10875 (2018/08/03)

Porous organic polymers (POPs) have attracted significant attention towards molecular adsorption in recent years due to their high porosity, diverse functionality and excellent chemical stability. In this work, we present a systematic case study on the fo

Microwave-activated synthesis of thiazolo[5,4-d]thiazoles by a condensation/oxidation sequence

Dessi, Alessio,Calamante, Massimo,Mordini, Alessandro,Zani, Lorenzo,Taddei, Maurizio,Reginato, Gianna

, p. 1322 - 1328 (2014/01/06)

A microwave-assisted preparation of symmetrical thiazolo[5,4-d]thiazoles from the corresponding aldehydes is presented. The two-step reaction sequence comprises the condensation of aldehydes with dithiooxamide followed by oxidation/aromatization with 1,4-

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