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2,6-Dithia-s-indacene-4,8-dione, a heterocyclic compound with the chemical formula C8H4O2S2, is characterized by the presence of two sulfur atoms and a carbonyl group. This unique structure endows it with distinctive properties, making it a promising candidate for various applications in organic synthesis, materials science, and electronic devices.

33527-23-0

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33527-23-0 Usage

Uses

Used in Organic Synthesis:
2,6-Dithia-s-indacene-4,8-dione serves as a versatile building block for the synthesis of a wide range of organic compounds. Its unique structure allows for the formation of various functional groups and molecular architectures, facilitating the development of novel chemical entities with potential applications in pharmaceuticals, agrochemicals, and other industries.
Used in Materials Science:
Due to its distinctive properties, 2,6-Dithia-s-indacene-4,8-dione has potential applications in the development of advanced materials for various purposes. Its incorporation into polymers, coatings, and other materials can enhance their performance, durability, and functionality.
Used as a Fluorescent Probe in Research:
2,6-Dithia-s-indacene-4,8-dione's fluorescent properties make it a valuable tool in biological and chemical research. It can be used as a fluorescent probe to study molecular interactions, monitor chemical reactions, and visualize biological processes at the molecular level.
Used in Organic Light-Emitting Diodes (OLEDs):
2,6-Dithia-s-indacene-4,8-dione's electronic properties have been studied for potential use in organic light-emitting diodes (OLEDs), which are widely used in display technologies and lighting applications. Incorporating 2,6-Dithia-s-indacene-4,8-dione into OLED devices could improve their efficiency, brightness, and color quality.
Used in Electronic Devices:
Beyond OLEDs, 2,6-Dithia-s-indacene-4,8-dione's electronic properties also make it a candidate for other electronic devices, such as sensors, transistors, and solar cells. Its integration into these devices could enhance their performance and contribute to the development of next-generation technologies.

Check Digit Verification of cas no

The CAS Registry Mumber 33527-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,2 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33527-23:
(7*3)+(6*3)+(5*5)+(4*2)+(3*7)+(2*2)+(1*3)=100
100 % 10 = 0
So 33527-23-0 is a valid CAS Registry Number.

33527-23-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name thieno[3,4-f][2]benzothiole-4,8-dione

1.2 Other means of identification

Product number -
Other names 4,8-dihidrobenzo<1,2-c:4,5-c'>dithiophene-4,8-dione

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:33527-23-0 SDS

33527-23-0Upstream product

33527-23-0Relevant academic research and scientific papers

Synthetic Entry to Polyfunctionalized Molecules through the [3+2]-Cycloaddition of Thiocarbonyl Ylides

Habiger, Christoph,Haut, Franz-Lucas,Korber, Johannes Nepomuk,Müller, Thomas,Magauer, Thomas,Mayer, Peter,Speck, Klaus,Wurst, Klaus

supporting information, (2019/09/06)

Here we present a comprehensive study on the [3+2]-cycloaddition of thiocarbonyl ylides with a wide variety of alkenes and alkynes. The obtained dihydro- and tetrahydrothiophene products serve as exceptionally versatile intermediates providing access to thiophenes, dienes, dendralenes, and vic-quarternary carbon centers. The use of high-pressure conditions enables thermally unstable, sterically encumbered or moderately reactive substrates to undergo the cycloaddition under mild conditions, thereby increasing the yield by up to 58percent. In addition, we showcase its utility by the formal syntheses of the pharmaceuticals NGB 4420 and tenilapine.

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