Cas 107438-90-4,8-Ethoxy-2-pentafluorobenzenesulfonyl-4-(toluene-4-sulfonyl)-2-aza-bicyclo[2.2.2]oct-5-en-3-one

107438-90-4

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Basic information

Product Name: 8-Ethoxy-2-pentafluorobenzenesulfonyl-4-(toluene-4-sulfonyl)-2-aza-bicyclo[2.2.2]oct-5-en-3-one
Synonyms:
CAS NO:107438-90-4
Molecular Formula:
Molecular Weight: 551.512
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 8-Ethoxy-2-pentafluorobenzenesulfonyl-4-(toluene-4-sulfonyl)-2-aza-bicyclo[2.2.2]oct-5-en-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 8-Ethoxy-2-pentafluorobenzenesulfonyl-4-(toluene-4-sulfonyl)-2-aza-bicyclo[2.2.2]oct-5-en-3-one(107438-90-4)
EPA Substance Registry System: 8-Ethoxy-2-pentafluorobenzenesulfonyl-4-(toluene-4-sulfonyl)-2-aza-bicyclo[2.2.2]oct-5-en-3-one(107438-90-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 107438-90-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107438-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,4,3 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107438-90:
(8*1)+(7*0)+(6*7)+(5*4)+(4*3)+(3*8)+(2*9)+(1*0)=124
124 % 10 = 4
So 107438-90-4 is a valid CAS Registry Number.

107438-90-4Upstream product

107438-90-4Downstream Products

107438-90-4Relevant academic research and scientific papers

Diels-Alder Cycloadditions Using Electrophilic Sulfonylpyridones

Posner, Gary H.,Switzer, Christopher

, p. 1642 - 1644 (1987)

Examples are presented of 5-7-kbar -cycloadditions of electrophilic 1,3-disulfonyl-2-pyridones with vinyl ethers leading regioselectively and stereoselectively to unsaturated, bridged, bicyclic lactams and, ultimately, to polyfunctionalized cyclohe

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