Cas 1569313-76-3,triisopropyl(((1R,2S,3R,5R)-3-methyl-1-vinyl-6-oxabicyclo[3.1.0]hexan-2-yl)oxy)silane

1569313-76-3

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Basic information

Product Name: triisopropyl(((1R,2S,3R,5R)-3-methyl-1-vinyl-6-oxabicyclo[3.1.0]hexan-2-yl)oxy)silane
Synonyms: triisopropyl(((1R,2S,3R,5R)-3-methyl-1-vinyl-6-oxabicyclo[3.1.0]hexan-2-yl)oxy)silane
CAS NO:1569313-76-3
Molecular Formula:
Molecular Weight: 296.525
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: triisopropyl(((1R,2S,3R,5R)-3-methyl-1-vinyl-6-oxabicyclo[3.1.0]hexan-2-yl)oxy)silane(CAS DataBase Reference)
NIST Chemistry Reference: triisopropyl(((1R,2S,3R,5R)-3-methyl-1-vinyl-6-oxabicyclo[3.1.0]hexan-2-yl)oxy)silane(1569313-76-3)
EPA Substance Registry System: triisopropyl(((1R,2S,3R,5R)-3-methyl-1-vinyl-6-oxabicyclo[3.1.0]hexan-2-yl)oxy)silane(1569313-76-3)

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: 1569313-76-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1569313-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,3,1 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1569313-76:
(9*1)+(8*5)+(7*6)+(6*9)+(5*3)+(4*1)+(3*3)+(2*7)+(1*6)=193
193 % 10 = 3
So 1569313-76-3 is a valid CAS Registry Number.

1569313-76-3Upstream product

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1569313-76-3Relevant academic research and scientific papers

Enyne metathesis approach towards the cyclopentane motif of jatrophane diterpenes

Lentsch, Christoph,Fürst, Rita,Rinner, Uwe

, p. 2665 - 2670 (2013)

A short and efficient synthesis of the cyclopentane moiety of the jatrophane diterpene Pl-3 has been developed. The route features an enyne metathesis reaction, and a stereoselective palladium-catalyzed reductive epoxide opening as key steps. Georg Thieme Verlag Stuttgart New York.

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