Cas 1326239-58-0,1-(3,5-bis(trifluoromethyl)phenyl)-3-((1R)-(6-methoxyquinolin-4-yl)(3-vinylquinuclidin-7-yl)methyl)urea

1326239-58-0

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Basic information

Product Name: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1R)-(6-methoxyquinolin-4-yl)(3-vinylquinuclidin-7-yl)methyl)urea
Synonyms:
CAS NO:1326239-58-0
Molecular Formula:
Molecular Weight: 472.587
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: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1R)-(6-methoxyquinolin-4-yl)(3-vinylquinuclidin-7-yl)methyl)urea(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1R)-(6-methoxyquinolin-4-yl)(3-vinylquinuclidin-7-yl)methyl)urea(1326239-58-0)
EPA Substance Registry System: 1-(3,5-bis(trifluoromethyl)phenyl)-3-((1R)-(6-methoxyquinolin-4-yl)(3-vinylquinuclidin-7-yl)methyl)urea(1326239-58-0)

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: 1326239-58-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1326239-58-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,6,2,3 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1326239-58:
(9*1)+(8*3)+(7*2)+(6*6)+(5*2)+(4*3)+(3*9)+(2*5)+(1*8)=150
150 % 10 = 0
So 1326239-58-0 is a valid CAS Registry Number.

1326239-58-0Upstream product

56-54-2 quinine

1326239-58-0Downstream Products

1326239-58-0Relevant academic research and scientific papers

Enantioselective organocatalytic aryloxylation of β-keto esters

Greenaway, Kevin,Dambruoso, Paolo,Ferrali, Alessandro,Hazelwood, Andrew J.,Sladojevich, Filippo,Dixon, Darren J.

, p. 1880 - 1886 (2011)

An efficient enantioselective aryloxylation of cyclic β-keto esters with a selection of substituted o-quinones catalyzed by a bifunctional cinchona alkaloid derivative, giving entry to tricyclic dioxin adducts with high enantio- and diastereoselectivity, is described. Georg Thieme Verlag Stuttgart - New York.

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