Cas 1294477-90-9,(3aR,4S,6R,6aS)-2-tosyl-4-(3-(trimethylsilyl)prop-1-enyl)-6-vinyloctahydrocyclopenta[c]pyrrole

1294477-90-9

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Basic information

Product Name: (3aR,4S,6R,6aS)-2-tosyl-4-(3-(trimethylsilyl)prop-1-enyl)-6-vinyloctahydrocyclopenta[c]pyrrole
Synonyms:
CAS NO:1294477-90-9
Molecular Formula:
Molecular Weight: 403.661
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: (3aR,4S,6R,6aS)-2-tosyl-4-(3-(trimethylsilyl)prop-1-enyl)-6-vinyloctahydrocyclopenta[c]pyrrole(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,4S,6R,6aS)-2-tosyl-4-(3-(trimethylsilyl)prop-1-enyl)-6-vinyloctahydrocyclopenta[c]pyrrole(1294477-90-9)
EPA Substance Registry System: (3aR,4S,6R,6aS)-2-tosyl-4-(3-(trimethylsilyl)prop-1-enyl)-6-vinyloctahydrocyclopenta[c]pyrrole(1294477-90-9)

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: 1294477-90-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1294477-90-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,4,4,7 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1294477-90:
(9*1)+(8*2)+(7*9)+(6*4)+(5*4)+(4*7)+(3*7)+(2*9)+(1*0)=199
199 % 10 = 9
So 1294477-90-9 is a valid CAS Registry Number.

1294477-90-9Upstream product

1294477-90-9Downstream Products

1294477-90-9Relevant academic research and scientific papers

A novel ligand for the enantioselective ruthenium-catalyzed olefin metathesis

Kannenberg, Axel,Rost, Daniel,Eibauer, Stefan,Tiede, Sascha,Blechert, Siegfried

, p. 3299 - 3302 (2011)

A bridge connects and efficiently transfers the chirality from the backbone of a N-heterocyclic carbene (NHC) to the metal center. The result is excellent enantioselectivities in the ruthenium-catalyzed, asymmetric ring-opening cross-metathesis of norborn

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