56714-11-5

Basic information

• Product Name: 1,3,3a,4,9,9a-hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide
• Synonyms: 1,3,3a,4,9,9a-Hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide; thieno[3,4-b]quinoxaline, 1,3,3a,4,9,9a-hexahydro-, 2,2-dioxide
• CAS NO: 56714-11-5
• Molecular Formula: C₁₀H₁₂N₂O₂S
• Molecular Weight: 224.2795
• Mol File: 56714-11-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 523.6°C at 760 mmHg
• Flash Point: 270.5°C
• Density: 1.326g/cm³
• Vapor Pressure: 4.65E-11mmHg at 25°C
• Refractive Index: 1.592
• CAS DataBase Reference: 1,3,3a,4,9,9a-hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,3a,4,9,9a-hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide(56714-11-5)
• EPA Substance Registry System: 1,3,3a,4,9,9a-hexahydrothieno[3,4-b]quinoxaline 2,2-dioxide(56714-11-5)

Safety Data

• Hazardous Substances Data: 56714-11-5(Hazardous Substances Data)

Usage

Chemical structure

A tricyclic compound with a thienoquinoxaline core and a 2,2-dioxide group.

Redox cofactor

PQQ acts as a redox cofactor in various biological functions.

Cellular energy metabolism

PQQ plays a role in cellular energy metabolism by enhancing mitochondrial function.

Mitochondrial biogenesis

PQQ promotes the formation of new mitochondria in cells.

Antioxidant defense

PQQ has antioxidant properties, helping to protect cells from oxidative stress.

Cognitive function

PQQ has been studied for its potential to improve cognitive function and brain health.

Cardiovascular health

PQQ is being investigated for its potential role in supporting cardiovascular health.

Dietary supplement

PQQ is available as a dietary supplement for those seeking its potential health benefits.

Therapeutic applications

PQQ is being researched for its potential therapeutic applications in various health conditions.

Upstream product

• 15091-30-2 3,4-dibromo-2,3,4,5-tetrahydrothiophene-1,1-dioxide 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 129303-28-2 parachlorobenzoyl-4 hexahydro-1,3,3a,4,9,9a thieno <3,4-b> quinoxaline dioxyde-2,2 
• 159850-92-7 quinoxalino-<2,3-c>-cyclobutene 
• 2379-55-7 2,3-dimethylquinoxaline 

Relevant articles and documents

Generation and Chemical Reactions of Quinoxalino-o-quinodimethane

We have prepared the unsubstituted quinoxalino-3-sulfolene 7 via two convenient routes and discovered its unusual stability toward thermal extrusion of SO2.The generation of the o-quinodimethane 14 from 7 was achieved at temperatures higher than 290 deg C.