Cas 1362113-49-2,4-((R)-((2S,4S,8R)-8-ethylquinuclidin-2-yl)(tert-butyldiphenylsilyloxy)methyl)-6-methoxyquinolin-5-amine

1362113-49-2

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Basic information

Product Name: 4-((R)-((2S,4S,8R)-8-ethylquinuclidin-2-yl)(tert-butyldiphenylsilyloxy)methyl)-6-methoxyquinolin-5-amine
Synonyms:
CAS NO:1362113-49-2
Molecular Formula:
Molecular Weight: 834.977
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: 4-((R)-((2S,4S,8R)-8-ethylquinuclidin-2-yl)(tert-butyldiphenylsilyloxy)methyl)-6-methoxyquinolin-5-amine(CAS DataBase Reference)
NIST Chemistry Reference: 4-((R)-((2S,4S,8R)-8-ethylquinuclidin-2-yl)(tert-butyldiphenylsilyloxy)methyl)-6-methoxyquinolin-5-amine(1362113-49-2)
EPA Substance Registry System: 4-((R)-((2S,4S,8R)-8-ethylquinuclidin-2-yl)(tert-butyldiphenylsilyloxy)methyl)-6-methoxyquinolin-5-amine(1362113-49-2)

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: 1362113-49-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1362113-49-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,2,1,1 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1362113-49:
(9*1)+(8*3)+(7*6)+(6*2)+(5*1)+(4*1)+(3*3)+(2*4)+(1*9)=122
122 % 10 = 2
So 1362113-49-2 is a valid CAS Registry Number.

1362113-49-2Upstream product

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1362113-49-2Relevant academic research and scientific papers

A novel C-5′ substituted cinchona alkaloid-derived catalyst promotes additions of alkyl thiols to nitroolefins with excellent enantioselectivity

Palacio, Carole,Connon, Stephen J.

supporting information; experimental part, p. 2849 - 2851 (2012/03/27)

A new bifunctional C-5′ substituted cinchona alkaloid-based catalyst promotes the first highly enantioselective additions of alkyl thiols to nitrostyrenes. The Royal Society of Chemistry 2012.

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