Cas 293291-04-0,[2-(1-benzyloxy-1-vinyl-allyl)-2-(2-tert-butyldimethylsiloxy)ethyl-hex-5-enyl]benzene

293291-04-0

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Basic information

Product Name: [2-(1-benzyloxy-1-vinyl-allyl)-2-(2-tert-butyldimethylsiloxy)ethyl-hex-5-enyl]benzene
Synonyms: [2-(1-benzyloxy-1-vinyl-allyl)-2-(2-tert-butyldimethylsiloxy)ethyl-hex-5-enyl]benzene
CAS NO:293291-04-0
Molecular Formula:
Molecular Weight: 490.802
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: [2-(1-benzyloxy-1-vinyl-allyl)-2-(2-tert-butyldimethylsiloxy)ethyl-hex-5-enyl]benzene(CAS DataBase Reference)
NIST Chemistry Reference: [2-(1-benzyloxy-1-vinyl-allyl)-2-(2-tert-butyldimethylsiloxy)ethyl-hex-5-enyl]benzene(293291-04-0)
EPA Substance Registry System: [2-(1-benzyloxy-1-vinyl-allyl)-2-(2-tert-butyldimethylsiloxy)ethyl-hex-5-enyl]benzene(293291-04-0)

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: 293291-04-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 293291-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,2,9 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 293291-04:
(8*2)+(7*9)+(6*3)+(5*2)+(4*9)+(3*1)+(2*0)+(1*4)=150
150 % 10 = 0
So 293291-04-0 is a valid CAS Registry Number.

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293291-04-0Downstream Products

293291-04-0Relevant academic research and scientific papers

Diastereoselective double ring closing metathesis reactions as an approach to symmetrical bicyclodienes

Lautens,Hughes,Zunic

, p. 868 - 883 (2007/10/03)

A new class of bicyclic dienes which contain a σ plane of symmetry are efficiently prepared in a diastereoselective fashion using ring closing metathesis reactions. These molecules have potential as starting materials for a wide range of organic targets.

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