Cas 492450-87-0,<i>tert</i>-butyl-{3,5-dimethoxy-2-[3-(2-methoxy-phenyl)-allyl]-phenoxy}-dimethyl-silane

492450-87-0

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Basic information

Product Name: tert-butyl-{3,5-dimethoxy-2-[3-(2-methoxy-phenyl)-allyl]-phenoxy}-dimethyl-silane
Synonyms: tert-butyl-{3,5-dimethoxy-2-[3-(2-methoxy-phenyl)-allyl]-phenoxy}-dimethyl-silane
CAS NO:492450-87-0
Molecular Formula:
Molecular Weight: 414.617
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: tert-butyl-{3,5-dimethoxy-2-[3-(2-methoxy-phenyl)-allyl]-phenoxy}-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl-{3,5-dimethoxy-2-[3-(2-methoxy-phenyl)-allyl]-phenoxy}-dimethyl-silane(492450-87-0)
EPA Substance Registry System: tert-butyl-{3,5-dimethoxy-2-[3-(2-methoxy-phenyl)-allyl]-phenoxy}-dimethyl-silane(492450-87-0)

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: 492450-87-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 492450-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,2,4,5 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 492450-87:
(8*4)+(7*9)+(6*2)+(5*4)+(4*5)+(3*0)+(2*8)+(1*7)=170
170 % 10 = 0
So 492450-87-0 is a valid CAS Registry Number.

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492450-87-0Relevant academic research and scientific papers

Ruthenium-catalyzed olefin cross metathesis of styrenes as an alternative to the Heck and cross-coupling reactions

Chatterjee, Arnab K.,Toste, F. Dean,Choi, Tae-Lim,Grubbs, Robert H.

, p. 634 - 637 (2002)

The use of olefin cross metathesis as a method for the formation of styrenyl-olefins is described using allylic substituted olefins and electron-deficient olefins. These methods provide an orthogonal method to alternative olefination strategies, such as the Heck reaction. These methods have also been employed in the total synthesis of 3-flavanols.

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