Cas 475299-67-3,ethyl (1R,3S,4S)-2-[(1R)-phenylethyl]-2-azabicyclo[2.2.2]oct-5-ene-3-carboxylate

475299-67-3

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Basic information

Product Name: ethyl (1R,3S,4S)-2-[(1R)-phenylethyl]-2-azabicyclo[2.2.2]oct-5-ene-3-carboxylate
Synonyms: ethyl (1R,3S,4S)-2-[(1R)-phenylethyl]-2-azabicyclo[2.2.2]oct-5-ene-3-carboxylate
CAS NO:475299-67-3
Molecular Formula:
Molecular Weight: 285.386
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: ethyl (1R,3S,4S)-2-[(1R)-phenylethyl]-2-azabicyclo[2.2.2]oct-5-ene-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (1R,3S,4S)-2-[(1R)-phenylethyl]-2-azabicyclo[2.2.2]oct-5-ene-3-carboxylate(475299-67-3)
EPA Substance Registry System: ethyl (1R,3S,4S)-2-[(1R)-phenylethyl]-2-azabicyclo[2.2.2]oct-5-ene-3-carboxylate(475299-67-3)

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: 475299-67-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 475299-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,2,9 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 475299-67:
(8*4)+(7*7)+(6*5)+(5*2)+(4*9)+(3*9)+(2*6)+(1*7)=203
203 % 10 = 3
So 475299-67-3 is a valid CAS Registry Number.

475299-67-3Upstream product

475299-67-3Downstream Products

697289-68-2 ethyl (1R,3S,4R,5R,6S)-5,6-dihydroxy-2-azabicyclo[2.2.2]octane-3-carboxylate

475299-67-3Relevant academic research and scientific papers

A short stereoselective synthesis of disubstituted cyclic amino acids

Maison, Wolfgang,Adiwidjaja, Gunadi

, p. 5957 - 5960 (2002)

A new synthetic route to enantiomerically pure disubstituted derivatives of cyclic amino acids is reported. Key step of this synthesis is an oxidative cleavage of azabicycloalkene precursors that are synthesized in enantiomerically pure form via aza-Diels

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