34106-68-8

Basic information

• Product Name: ethyl 3-thia-6-azabicyclo[3.1.0]hexane-6-carboxylate 3,3-dioxide
• CAS NO: 34106-68-8
• Molecular Formula: C₇H₁₁NO₄S
• Molecular Weight: 205.2315
• Mol File: 34106-68-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 405.3°C at 760 mmHg
• Flash Point: 198.9°C
• Density: 1.474g/cm³
• Vapor Pressure: 8.84E-07mmHg at 25°C
• Refractive Index: 1.557
• CAS DataBase Reference: ethyl 3-thia-6-azabicyclo[3.1.0]hexane-6-carboxylate 3,3-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 3-thia-6-azabicyclo[3.1.0]hexane-6-carboxylate 3,3-dioxide(34106-68-8)
• EPA Substance Registry System: ethyl 3-thia-6-azabicyclo[3.1.0]hexane-6-carboxylate 3,3-dioxide(34106-68-8)

Safety Data

• Hazardous Substances Data: 34106-68-8(Hazardous Substances Data)

Upstream product

• 77-79-2 3-Sulfolene 
• 817-87-8 ethyl azidocarbonate 
• 22818-81-1 n-ethoxycarbonyl-p-nitrobenzene sulfonamide 

Relevant articles and documents

CHEMICAL REPERCUSSIONS OF ORBITAL INTERACTIONS THROUGH BOND AND THROUGH SPACE. THE REACTIVITY OF THE DOUBLE BOND IN UNSATURATED CYCLIC SULPHONES TOWARDS AZIRIDINE FORMATION AND EPOXIDATION

The ease of formation of aziridine and/or epoxides from a series of bicyclic olefins, where distant sulphonyl groups are present, is very variable.There is some correlation between reactivity of the vinyl group and its ?-ionisation potential which is high in the present molecules relative to comperison olefins.This increase is thought to be due to the presence of orbital interactions through bonds and/or through space between the sulphone group and the double bond, making the latter electron deficient.The ionisations potentials were determined by UV-photoelectron spectroscopy and the assignments made by recourse to ab initio configuration interaction methods.