Cas 86448-18-2,{2-[(1S,4S)-7-(2-Methyl-[1,3]dioxolan-2-yl)-2-aza-bicyclo[2.2.2]oct-5-en-2-yl]-4-oxo-cyclohex-2-enyl}-acetic acid ethyl ester

86448-18-2

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Basic information

Product Name: {2-[(1S,4S)-7-(2-Methyl-[1,3]dioxolan-2-yl)-2-aza-bicyclo[2.2.2]oct-5-en-2-yl]-4-oxo-cyclohex-2-enyl}-acetic acid ethyl ester
Synonyms:
CAS NO:86448-18-2
Molecular Formula:
Molecular Weight: 375.465
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: {2-[(1S,4S)-7-(2-Methyl-[1,3]dioxolan-2-yl)-2-aza-bicyclo[2.2.2]oct-5-en-2-yl]-4-oxo-cyclohex-2-enyl}-acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {2-[(1S,4S)-7-(2-Methyl-[1,3]dioxolan-2-yl)-2-aza-bicyclo[2.2.2]oct-5-en-2-yl]-4-oxo-cyclohex-2-enyl}-acetic acid ethyl ester(86448-18-2)
EPA Substance Registry System: {2-[(1S,4S)-7-(2-Methyl-[1,3]dioxolan-2-yl)-2-aza-bicyclo[2.2.2]oct-5-en-2-yl]-4-oxo-cyclohex-2-enyl}-acetic acid ethyl ester(86448-18-2)

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: 86448-18-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 86448-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,4 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86448-18:
(7*8)+(6*6)+(5*4)+(4*4)+(3*8)+(2*1)+(1*8)=162
162 % 10 = 2
So 86448-18-2 is a valid CAS Registry Number.

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86448-18-2Relevant academic research and scientific papers

MECHANISTIC AND SYNTHETIC ASPECTS OF THE ACID-CATALYZED AMINO-CLAISEN REARRANGEMENT OF N-(β-KETOVINYL)ISOQUINUCLIDENES.

Chen, Yuhpyng,Huesmann, Peter L.,Mariano, Patrick S.

, p. 1021 - 1024 (2007/10/02)

Srudies of the acid-catalyzed, amino-Claisen rearrangement of N-(β-cyclohexenonyl)isoquinuclidines have provided results which pertain to the mechanism of the process and to synthetic applications for construction of the lycorane tetracyclic skeleton.

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