768-10-5

Usage

Structure

Five-membered heterocyclic compound containing one sulfur (S), two nitrogen (N), and two carbon (C) atoms.

Electron-accepting properties

BTO is known for its ability to accept electrons, making it a suitable material for use in organic electronic devices.

Applications

BTO is commonly used as an acceptor material in organic solar cells and organic light-emitting diodes (OLEDs).

High electron affinity

BTO has a high electron affinity, which allows it to form stable radical anions.

Suitability for organic electronics

Due to its high electron affinity and ability to form stable radical anions, BTO is suitable for use in various organic electronic applications.

Potential as a fluorescence probe

BTO has potential for use as a fluorescence probe, which could be beneficial in biological imaging and sensing applications.

Upstream product

• 1753-21-5 5-Ethoxy-2,1,3-benzothiadiazole 
• 102-51-2 4-methoxy-1,2-phenylenediamine 
• 2207-32-1 5-chloro-2,1,3-benzothiadiazole 
• 99-56-9 4-Nitrophenylene-1,2-diamine 
• 16252-88-3 5-nitro-2,1,3-benzothiadiazole 
• 874-37-3 benzo[1,2,5]thiadiazol-5-ylamine 
• 1753-75-9 5-bromobenzo[c][1,2,5]thiadiazole 
• 1168135-03-2 5-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzo[c][1,2,5]thiodiazole 
• 95-83-0 4-Chloro-1,2-phenylenediamine 
• 5448-43-1 6-chloroquinoxaline 
• 1753-76-0 5-Methoxy-2,1,3-benzothiadiazol 
• 1197-37-1 4-ethoxy-benzene-1,2-diamine 

Downstream Products

• 1753-76-0 5-Methoxy-2,1,3-benzothiadiazol 
• 91330-58-4 4-phenylazo-benzo[1,2,5]thiadiazol-5-ol 
• 1753-21-5 5-Ethoxy-2,1,3-benzothiadiazole 
• 29123-11-3 Benz-2,1,3-thiodiazol-5-hydroxy-essigsaeure 
• 32863-29-9 4-Nitro-5-hydroxybenz-2,1,3-thiadiazol 
• 874-37-3 benzo[1,2,5]thiadiazol-5-ylamine 
• 847054-44-8 5-(4-nitro-phenoxy)-benzo[1,2,5]thiadiazol 
• 3177-69-3 4-Amino-5-hydroxy-2.1.3-benzothiadiazol 
• 615-72-5 3,4-diaminophenol 

Relevant academic research and scientific papers

A Monophosphine Ligand Derived from Anthracene Photodimer: Synthetic Applications for Palladium-Catalyzed Coupling Reactions

Herein, we present an air-stable dianthracenyl monophosphine ligand (diAnthPhos) which can be prepared in two steps from commercially available anthracene derivatives. The ligand exhibits excellent efficiency for palladium-catalyzed coupling reactions. In particular, Miyaura borylation of heterocycle-containing electrophiles can be facilitated employing the diAnthPhos ligand with a broad substrate scope and low catalyst loading. The valuable synthetic utility of the new ligand is further demonstrated by a one-pot Miyaura borylation/Suzuki coupling protocol for heteroaryl-containing substrates.

Benzothiadiazole compound and preparation method and use thereof

The present invention relates to a benzothiadiazole compound represented by the following formula I, and a preparation method and use thereof, the benzothiadiazole compound has the biological activityof inhibiting protein-tyrosine-phosphatase SHP2, can be used as a tool compound to study the biological functional relevance of the protein-tyrosine-phosphatase SHP2 in a cell signal transduction process, and provides a new means for prevention and treatment of cancer and metabolic and immune diseases.

Open-Resonance-Assisted Hydrogen Bonds and Competing Quasiaromaticity

The delocalization of electron density upon tautomerization of a proton across a conjugated bridge can alter the strength of hydrogen bonds. This effect has been dubbed resonance-assisted hydrogen bonding (RAHB) and plays a major role in the energetics of the tautomeric equilibrium. The goal of this work was to investigate the role that π-delocalization plays in the stability of RAHBs by engaging other isomerization processes. Similarly, acid-base chemistry has received little experimental attention in studies of RAHB, and we address the role that acid-base effects play in the tautomeric equilibrium. We find that π-delocalization and the disruption of adjacent aromatic rings is the dominant effect in determining the stability of a RAHB.

Palladium-catalyzed hydroxylation of aryl and heteroaryl halides enabled by the use of a palladacycle precatalyst

A method for the hydroxylation of aryl and heteroaryl halides, promoted by a catalyst based on a biarylphosphine ligand tBuBrettPhos (L5) and its corresponding palladium precatalyst (1), is described. The reactions allow the cross-coupling of both potassium and cesium hydroxides with (hetero)aryl halides to afford a variety of phenols and hydroxylated heteroarenes in high to excellent yield.

Nicotinamide benzofused-heterocyclyl derivatives useful as selective inhibitors of pde4 isozymes

Compounds useful as inhibitors of PDE4 in the treatment of diseases regulated by the activation and degranulation of eosinophils, especially asthma, chronic bronchitis, and chronic obstructive pulmonary disease, of Formula (1.0.0): 1 wherein R5 and R6 are