Cas 196493-34-2,13-methyl-10,11-dioxatricyclo[7.2.2.0<sup>2,7</sup>]trideca-2,4,6,12-tetraene

196493-34-2

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Basic information

Product Name: 13-methyl-10,11-dioxatricyclo[7.2.2.0^2,7]trideca-2,4,6,12-tetraene
Synonyms: 13-methyl-10,11-dioxatricyclo[7.2.2.0^2,7]trideca-2,4,6,12-tetraene
CAS NO:196493-34-2
Molecular Formula:
Molecular Weight: 188.226
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: 13-methyl-10,11-dioxatricyclo[7.2.2.0^2,7]trideca-2,4,6,12-tetraene(CAS DataBase Reference)
NIST Chemistry Reference: 13-methyl-10,11-dioxatricyclo[7.2.2.0^2,7]trideca-2,4,6,12-tetraene(196493-34-2)
EPA Substance Registry System: 13-methyl-10,11-dioxatricyclo[7.2.2.0^2,7]trideca-2,4,6,12-tetraene(196493-34-2)

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: 196493-34-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 196493-34-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,4,9 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 196493-34:
(8*1)+(7*9)+(6*6)+(5*4)+(4*9)+(3*3)+(2*3)+(1*4)=182
182 % 10 = 2
So 196493-34-2 is a valid CAS Registry Number.

196493-34-2Upstream product

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196493-34-2Relevant academic research and scientific papers

Unusual triethylamine catalyzed rearrangement of bicyclic endoperoxides derived from substituted cycloheptatrienes

Senguel, M. Emin,Ceylan, Zeynep,Balci, Metin

, p. 10401 - 10408 (1997)

Triethylamine catalyzed rearrangement of the substituted bicyclic cycloheptatriene endoperoxides 9, 10, 12, 13, 20, 21, 22 and 30 underwent different reaction modes and resulted in the formation of ring contraction products in the case of 9, 10, 12 and 13. However, 20, 21, and 30 provided rearranged diketones 23, 24 and 32 almost in quantitative yield. The mechanism of these reactions was discussed.

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