Cas 941703-60-2,1-((S)-quinolin-4-yl((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)-3-(4-(trifluoromethyl)phenyl)thiourea

941703-60-2

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Basic information

Product Name: 1-((S)-quinolin-4-yl((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)-3-(4-(trifluoromethyl)phenyl)thiourea
Synonyms: 1-((S)-quinolin-4-yl((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)-3-(4-(trifluoromethyl)phenyl)thiourea
CAS NO:941703-60-2
Molecular Formula:
Molecular Weight: 496.599
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-((S)-quinolin-4-yl((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)-3-(4-(trifluoromethyl)phenyl)thiourea(CAS DataBase Reference)
NIST Chemistry Reference: 1-((S)-quinolin-4-yl((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)-3-(4-(trifluoromethyl)phenyl)thiourea(941703-60-2)
EPA Substance Registry System: 1-((S)-quinolin-4-yl((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl)-3-(4-(trifluoromethyl)phenyl)thiourea(941703-60-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 941703-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 941703-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,1,7,0 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 941703-60:
(8*9)+(7*4)+(6*1)+(5*7)+(4*0)+(3*3)+(2*6)+(1*0)=162
162 % 10 = 2
So 941703-60-2 is a valid CAS Registry Number.

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941703-60-2Relevant academic research and scientific papers

Catalytic enantioselective iodoetherification of oximes

Tripathi, Chandra Bhushan,Mukherjee, Santanu

supporting information, p. 8450 - 8453 (2013/09/02)

Organocatalysis: The first catalytic enantioselective iodoetherification of oximes is developed using commercially available N-iodosuccinimide. In the presence of a dihydrocinchonidine-derived thiourea (10 mol %), β,γ-unsaturated oximes undergo facile iodoetherification to produce Δ2-isoxazolines containing a quaternary stereogenic center generally in high yield with good to excellent enantioselectivity. Copyright

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