Cas 1419351-65-7,benzyl ((E)-2-((2S,4R)-6-methoxy-2-(naphthalen-2-yl)-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate

1419351-65-7

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Basic information

Product Name: benzyl ((E)-2-((2S,4R)-6-methoxy-2-(naphthalen-2-yl)-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate
Synonyms: benzyl ((E)-2-((2S,4R)-6-methoxy-2-(naphthalen-2-yl)-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate
CAS NO:1419351-65-7
Molecular Formula:
Molecular Weight: 464.564
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: benzyl ((E)-2-((2S,4R)-6-methoxy-2-(naphthalen-2-yl)-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl ((E)-2-((2S,4R)-6-methoxy-2-(naphthalen-2-yl)-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate(1419351-65-7)
EPA Substance Registry System: benzyl ((E)-2-((2S,4R)-6-methoxy-2-(naphthalen-2-yl)-1,2,3,4-tetrahydroquinolin-4-yl)vinyl)carbamate(1419351-65-7)

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: 1419351-65-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1419351-65-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,9,3,5 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1419351-65:
(9*1)+(8*4)+(7*1)+(6*9)+(5*3)+(4*5)+(3*1)+(2*6)+(1*5)=157
157 % 10 = 7
So 1419351-65-7 is a valid CAS Registry Number.

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1419351-65-7Relevant academic research and scientific papers

Catalytic highly enantioselective vinylogous Povarov reaction

Caruana, Lorenzo,Fochi, Mariafrancesca,Ranieri, Silvia,Mazzanti, Andrea,Bernardi, Luca

supporting information, p. 880 - 882 (2013/02/25)

The first example of a catalytic asymmetric vinylogous Povarov reaction is presented. 1-N-Acylamino-1,3-butadienes react selectively at their terminal double bond in the presence of a chiral phosphoric acid catalyst, delivering highly enantioenriched 1,2,3,4-tetrahydroquinolines bearing a synthetically versatile enecarbamate group at the 4-position. The Royal Society of Chemistry 2013.

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