Cas 905930-27-0,9-butyl-1,8-diphenyl-10-(toluene-4-sulfonyl)-11-oxa-tricyclo[6.2.1.0<sup>2,7</sup>]undeca-2<sup>(7)</sup>,3,5,9-tetraene

905930-27-0

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Basic information

Product Name: 9-butyl-1,8-diphenyl-10-(toluene-4-sulfonyl)-11-oxa-tricyclo[6.2.1.0^2,7]undeca-2⁽⁷⁾,3,5,9-tetraene
Synonyms: 9-butyl-1,8-diphenyl-10-(toluene-4-sulfonyl)-11-oxa-tricyclo[6.2.1.0^2,7]undeca-2⁽⁷⁾,3,5,9-tetraene
CAS NO:905930-27-0
Molecular Formula:
Molecular Weight: 506.665
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: 9-butyl-1,8-diphenyl-10-(toluene-4-sulfonyl)-11-oxa-tricyclo[6.2.1.0^2,7]undeca-2⁽⁷⁾,3,5,9-tetraene(CAS DataBase Reference)
NIST Chemistry Reference: 9-butyl-1,8-diphenyl-10-(toluene-4-sulfonyl)-11-oxa-tricyclo[6.2.1.0^2,7]undeca-2⁽⁷⁾,3,5,9-tetraene(905930-27-0)
EPA Substance Registry System: 9-butyl-1,8-diphenyl-10-(toluene-4-sulfonyl)-11-oxa-tricyclo[6.2.1.0^2,7]undeca-2⁽⁷⁾,3,5,9-tetraene(905930-27-0)

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: 905930-27-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 905930-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,9,3 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 905930-27:
(8*9)+(7*0)+(6*5)+(5*9)+(4*3)+(3*0)+(2*2)+(1*7)=170
170 % 10 = 0
So 905930-27-0 is a valid CAS Registry Number.

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905930-27-0Relevant academic research and scientific papers

Rearrangements of the Diels-Alder cycloadducts obtained from acetylenic sulfones and 1,3-diphenylisobenzofuran

Back, Thomas G.,Parvez, Masood,Zhai, Huimin

, p. 5254 - 5259 (2006)

1,3-Diphenylisobenzofuran afforded Diels-Alder cycloadducts 4a,b with n-butyl- and phenyl-substituted acetylenic sulfones 3a,b, respectively. The products underwent various types of rearrangements under pyrolytic, acid-catalyzed, and photochemical conditi

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