Cas 1617568-11-2,isopropyl (R)-2-((R)-2-(methoxycarbonyl)-1-phenylallyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

1617568-11-2

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Basic information

Product Name: isopropyl (R)-2-((R)-2-(methoxycarbonyl)-1-phenylallyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate
Synonyms:
CAS NO:1617568-11-2
Molecular Formula:
Molecular Weight: 392.452
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: isopropyl (R)-2-((R)-2-(methoxycarbonyl)-1-phenylallyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: isopropyl (R)-2-((R)-2-(methoxycarbonyl)-1-phenylallyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate(1617568-11-2)
EPA Substance Registry System: isopropyl (R)-2-((R)-2-(methoxycarbonyl)-1-phenylallyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate(1617568-11-2)

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: 1617568-11-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1617568-11-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,7,5,6 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1617568-11:
(9*1)+(8*6)+(7*1)+(6*7)+(5*5)+(4*6)+(3*8)+(2*1)+(1*1)=182
182 % 10 = 2
So 1617568-11-2 is a valid CAS Registry Number.

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1617568-11-2Relevant academic research and scientific papers

Organocatalytic enantioselective allylic alkylation of MBH carbonates with β-keto esters

Kamlar,Hybelbauerova,Cisarova,Vesely

supporting information, p. 5071 - 5076 (2014/07/08)

The highly stereoselective allylic alkylation of Morita-Baylis-Hillman carbonates with β-ketoesters catalysed by β-ICD is described. The corresponding products containing two adjacent quaternary and tertiary carbon centers were obtained in good yields with high diastereoselectivity (up to 10 : 1 dr) and enantioselectivity (up to 95% ee).

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