Cas 78133-65-0,(1R,2R,6S,7S,10S)-1-Methyl-4-phenyl-10-trimethylsilanyl-4-aza-tricyclo[5.2.1.0<sup>2,6</sup>]dec-8-ene-3,5-dione

78133-65-0

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Basic information

Product Name: (1R,2R,6S,7S,10S)-1-Methyl-4-phenyl-10-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione
Synonyms:
CAS NO:78133-65-0
Molecular Formula:
Molecular Weight: 325.483
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: (1R,2R,6S,7S,10S)-1-Methyl-4-phenyl-10-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,6S,7S,10S)-1-Methyl-4-phenyl-10-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione(78133-65-0)
EPA Substance Registry System: (1R,2R,6S,7S,10S)-1-Methyl-4-phenyl-10-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione(78133-65-0)

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 78133-65-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78133-65-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,3 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 78133-65:
(7*7)+(6*8)+(5*1)+(4*3)+(3*3)+(2*6)+(1*5)=140
140 % 10 = 0
So 78133-65-0 is a valid CAS Registry Number.

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78133-65-0Relevant academic research and scientific papers

The Reaction between Bis(trimethylsilyl)cyclopentadiene and Dichloroketen, and the Diels-Alder Reactions between N-Phenylmaleimide and Two Silylated Methylcyclopentadienes

Fleming, Ian,Williams, Richard Vaughan

, p. 684 - 688 (2007/10/02)

Bis(trimethylsilyl)cyclopentadiene reacts with dichloroketen to give only the adduct (7) derived from the 2,5-disilylated isomer (5).Methyl(trimethylsilyl)cyclopentadiene (18) and trimethylsilylmethylcyclopentadiene (21) give Diels-Alder adducts (19) and (20) and (22) and (23) in which the regioselectivity is unaffected by the presence of the silyl group.Epoxidation of the edduct (22) and acid-catalysed opening of the epoxide lead to formation of the exo-methylenenorbornane (26) in a rearrangement controlled by the presence of the silyl group.

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