Cas 445433-08-9,(R)-((1S,2S,4S,5R)-5-{3-[(Z)-Benzylimino]-propyl}-1-aza-bicyclo[2.2.2]oct-2-yl)-quinolin-4-yl-methanol

445433-08-9

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Basic information

Product Name: (R)-((1S,2S,4S,5R)-5-{3-[(Z)-Benzylimino]-propyl}-1-aza-bicyclo[2.2.2]oct-2-yl)-quinolin-4-yl-methanol
Synonyms: (R)-((1S,2S,4S,5R)-5-{3-[(Z)-Benzylimino]-propyl}-1-aza-bicyclo[2.2.2]oct-2-yl)-quinolin-4-yl-methanol
CAS NO:445433-08-9
Molecular Formula:
Molecular Weight: 413.563
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: (R)-((1S,2S,4S,5R)-5-{3-[(Z)-Benzylimino]-propyl}-1-aza-bicyclo[2.2.2]oct-2-yl)-quinolin-4-yl-methanol(CAS DataBase Reference)
NIST Chemistry Reference: (R)-((1S,2S,4S,5R)-5-{3-[(Z)-Benzylimino]-propyl}-1-aza-bicyclo[2.2.2]oct-2-yl)-quinolin-4-yl-methanol(445433-08-9)
EPA Substance Registry System: (R)-((1S,2S,4S,5R)-5-{3-[(Z)-Benzylimino]-propyl}-1-aza-bicyclo[2.2.2]oct-2-yl)-quinolin-4-yl-methanol(445433-08-9)

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: 445433-08-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 445433-08-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,5,4,3 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 445433-08:
(8*4)+(7*4)+(6*5)+(5*4)+(4*3)+(3*3)+(2*0)+(1*8)=139
139 % 10 = 9
So 445433-08-9 is a valid CAS Registry Number.

445433-08-9Upstream product

445433-08-9Downstream Products

445433-08-9Relevant academic research and scientific papers

Highly selective hydroformylation of the Cinchona alkaloids

Lambers, Marielle,Beijer, Felix H.,Padron, Jose M.,Toth, Imre,de Vries, Johannes G.

, p. 5022 - 5024 (2002)

The four naturally occurring cinchona alkaloids were subjected to hydroformylation to create an extra functional group that allows immobilization. Cinchonidine, quinine, and quinidine, could be hydroformylated with virtually complete terminal selectivity, using a rhodium/tetraphosphite catalyst. The cinchonidine aldehyde was reduced to the alcohol and subjected to reductive amination with benzylamine.

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