Cas 286368-27-2,Methanesulfonic acid (1S,2S,4S,5S)-5-(4-nitro-phenylethynyl)-1-aza-bicyclo[2.2.2]oct-2-ylmethyl ester

286368-27-2

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Basic information

Product Name: Methanesulfonic acid (1S,2S,4S,5S)-5-(4-nitro-phenylethynyl)-1-aza-bicyclo[2.2.2]oct-2-ylmethyl ester
Synonyms: Methanesulfonic acid (1S,2S,4S,5S)-5-(4-nitro-phenylethynyl)-1-aza-bicyclo[2.2.2]oct-2-ylmethyl ester
CAS NO:286368-27-2
Molecular Formula:
Molecular Weight: 364.422
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: Methanesulfonic acid (1S,2S,4S,5S)-5-(4-nitro-phenylethynyl)-1-aza-bicyclo[2.2.2]oct-2-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Methanesulfonic acid (1S,2S,4S,5S)-5-(4-nitro-phenylethynyl)-1-aza-bicyclo[2.2.2]oct-2-ylmethyl ester(286368-27-2)
EPA Substance Registry System: Methanesulfonic acid (1S,2S,4S,5S)-5-(4-nitro-phenylethynyl)-1-aza-bicyclo[2.2.2]oct-2-ylmethyl ester(286368-27-2)

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: 286368-27-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 286368-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,6,3,6 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 286368-27:
(8*2)+(7*8)+(6*6)+(5*3)+(4*6)+(3*8)+(2*2)+(1*7)=182
182 % 10 = 2
So 286368-27-2 is a valid CAS Registry Number.

286368-27-2Upstream product

124-63-0 methanesulfonyl chloride

286368-27-2Downstream Products

286368-28-3 (1S,2S,4S,5S)-2-iodomethyl-5-(p-nitrophenylethynyl)-1-azabicyclo[2.2.2]octane

286368-27-2Relevant academic research and scientific papers

Synthesis of enantiopure 1-azabicyclo[3.2.2]nonanes via stereoselective capture of chiral carbocations.

Roeper,Frackenpohl,Schrake,Wartchow,Hoffmann

, p. 1661 - 1664 (2000)

[reaction: see text] A new class of doubly functionalized and enantiomerically pure 1-azabicyclo[3.2.2]nonanes derived from quincorine and quincoridine is described. 2,5-Disubstituted quinuclidines with a C9-mesyloxy group were easily transformed into the

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