122608-26-8

Basic information

• Product Name: 2a,2b,6b,6c-Tetrahydro-1-oxa-2-thiabenzocyclopropapentalene 2-Oxide
• Synonyms: 2a,2b,6b,6c-Tetrahydro-1-oxa-2-thiabenzocyclopropapentalene 2-Oxide
• CAS NO: 122608-26-8
• Molecular Weight: 192.238
• Mol File: 122608-26-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2a,2b,6b,6c-Tetrahydro-1-oxa-2-thiabenzocyclopropapentalene 2-Oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 2a,2b,6b,6c-Tetrahydro-1-oxa-2-thiabenzocyclopropapentalene 2-Oxide(122608-26-8)
• EPA Substance Registry System: 2a,2b,6b,6c-Tetrahydro-1-oxa-2-thiabenzocyclopropapentalene 2-Oxide(122608-26-8)

Usage

General Description

2a,2b,6b,6c-Tetrahydro-1-oxa-2-thiabenzocyclopropapentalene 2-Oxide is a complex chemical compound with a unique molecular structure. It contains both oxygen and sulfur atoms, as well as a cyclopropyl ring system. 2a,2b,6b,6c-Tetrahydro-1-oxa-2-thiabenzocyclopropapentalene 2-Oxide is a heterocyclic oxide, meaning it contains at least one oxygen atom within a ring of carbon atoms. Its exact uses and properties are not specified in the name, but it likely has potential applications in organic chemistry, pharmaceuticals, and materials science. Further research and analysis would be needed to fully understand the potential uses and effects of this chemical.

Upstream product

Upstream product

• 122608-25-7 1,1a,6,6a-Tetrahydro-1,6-epithiocyclopropindene 7,7-Dioxide 

Downstream Products

• 91-20-3 naphthalene 
• 60585-47-9 1H-indene-1-carboxaldehyde 
• 64391-31-7 1H-indene-3-carboxaldehyde 
• 95-13-6 1-indene 
• 34305-47-0 1,2,3-metheno-1H-indene-2,3-dihydro 
• 122608-25-7 1,1a,6,6a-Tetrahydro-1,6-epithiocyclopropindene 7,7-Dioxide 

Relevant articles and documents

THERMOLYSIS OF THE SULFUR DIOXIDE ADDUCTS OF BENZOBENZVALENE. THE 1,3-DIPOLAR BEHAVIOUR OF A SULFENE

Pyrolysis (fvp) of a strained γ-sultine (3) produced 1H-indene-1-carboxaldehyde (8) and naphthalene.The key step in the production of aldehyde (8) involves a 1,3-dipolar cycloreversion, as evidenced by the trapping of an intermediate sulfene (6) with methyl acrylate.A diradical pathway is proposed for the formation of naphthalene.