Cas 1185735-41-4,5-((1'S,2'S,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-phenyl-(E)-2-penten-4-ynoic acid ethyl ester

1185735-41-4

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Basic information

Product Name: 5-((1'S,2'S,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-phenyl-(E)-2-penten-4-ynoic acid ethyl ester
Synonyms:
CAS NO:1185735-41-4
Molecular Formula:
Molecular Weight: 339.434
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: 5-((1'S,2'S,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-phenyl-(E)-2-penten-4-ynoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 5-((1'S,2'S,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-phenyl-(E)-2-penten-4-ynoic acid ethyl ester(1185735-41-4)
EPA Substance Registry System: 5-((1'S,2'S,4'S,5'S)-2'-hydroxymethyl-1'-azabicyclo[2.2.2]oct-5'-yl)-3-phenyl-(E)-2-penten-4-ynoic acid ethyl ester(1185735-41-4)

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: 1185735-41-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1185735-41-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,7,3 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1185735-41:
(9*1)+(8*1)+(7*8)+(6*5)+(5*7)+(4*3)+(3*5)+(2*4)+(1*1)=174
174 % 10 = 4
So 1185735-41-4 is a valid CAS Registry Number.

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1185735-41-4Relevant academic research and scientific papers

Synthesis of new quinuclidine derivatives via Pd-mediated cross-coupling and cross-benzannulation reactions

T?t?s, Stefania,Fild, Manfred,Th?ne, Carsten,Grosu, Ion

, p. 6226 - 6235 (2011/03/20)

New functionalized quinuclidines were prepared via palladium-catalyzed addition reactions of terminal alkynes (donors) to internal alkynes (acceptors). The enantiopure terminal alkynes were derivatives of quincoridine and quincorine, two semi-natural Cinc

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