Cas 106435-52-3,4-(tert-Butyldimethylsilyloxy)-2-phenyl-3ac,4,7,7ac-tetrahydro-4r,7c-ethano-1H-pyrrolo<3,4-d>pyridin-1,3,6(2H,5H)-trion

106435-52-3

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Product Name: 4-(tert-Butyldimethylsilyloxy)-2-phenyl-3ac,4,7,7ac-tetrahydro-4r,7c-ethano-1H-pyrrolo<3,4-d>pyridin-1,3,6(2H,5H)-trion
Synonyms:
CAS NO:106435-52-3
Molecular Formula:
Molecular Weight: 400.55
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: 4-(tert-Butyldimethylsilyloxy)-2-phenyl-3ac,4,7,7ac-tetrahydro-4r,7c-ethano-1H-pyrrolo<3,4-d>pyridin-1,3,6(2H,5H)-trion(CAS DataBase Reference)
NIST Chemistry Reference: 4-(tert-Butyldimethylsilyloxy)-2-phenyl-3ac,4,7,7ac-tetrahydro-4r,7c-ethano-1H-pyrrolo<3,4-d>pyridin-1,3,6(2H,5H)-trion(106435-52-3)
EPA Substance Registry System: 4-(tert-Butyldimethylsilyloxy)-2-phenyl-3ac,4,7,7ac-tetrahydro-4r,7c-ethano-1H-pyrrolo<3,4-d>pyridin-1,3,6(2H,5H)-trion(106435-52-3)

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: 106435-52-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 106435-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,4,3 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106435-52:
(8*1)+(7*0)+(6*6)+(5*4)+(4*3)+(3*5)+(2*5)+(1*2)=103
103 % 10 = 3
So 106435-52-3 is a valid CAS Registry Number.

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106435-52-3Relevant academic research and scientific papers

Synthesis and Reactions of 2,6-Bis(tert-butyldimethylsilyloxy)-3,4-dihydropyridine, a New, Reactive Heterodiene

Ried, Walter,Reiher, Uwe

, p. 657 - 658 (2007/10/02)

2,6-Bis(tert-butyldimethylsilyloxy)-3,4-dihydropyridine (2) is synthesized by double silylation of glutarimide (1).Diels-Alder reactions of 2 with various dienophiles lead to the adducts 3a-c, 5, and 7.By hydrolysis of these compounds the new heterocycles 4a-c, 6, and 8 are obtained.

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