Cas 206438-96-2,Acetic acid (R)-2-phenyl-1-((1R,2S,6R,7S)-1,10,10-trimethyl-3-oxa-5-aza-tricyclo[5.2.1.0<sup>2,6</sup>]dec-4-en-4-yl)-ethyl ester

206438-96-2

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Basic information

Product Name: Acetic acid (R)-2-phenyl-1-((1R,2S,6R,7S)-1,10,10-trimethyl-3-oxa-5-aza-tricyclo[5.2.1.0^2,6]dec-4-en-4-yl)-ethyl ester
Synonyms: Acetic acid (R)-2-phenyl-1-((1R,2S,6R,7S)-1,10,10-trimethyl-3-oxa-5-aza-tricyclo[5.2.1.0^2,6]dec-4-en-4-yl)-ethyl ester
CAS NO:206438-96-2
Molecular Formula:
Molecular Weight: 341.45
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: Acetic acid (R)-2-phenyl-1-((1R,2S,6R,7S)-1,10,10-trimethyl-3-oxa-5-aza-tricyclo[5.2.1.0^2,6]dec-4-en-4-yl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (R)-2-phenyl-1-((1R,2S,6R,7S)-1,10,10-trimethyl-3-oxa-5-aza-tricyclo[5.2.1.0^2,6]dec-4-en-4-yl)-ethyl ester(206438-96-2)
EPA Substance Registry System: Acetic acid (R)-2-phenyl-1-((1R,2S,6R,7S)-1,10,10-trimethyl-3-oxa-5-aza-tricyclo[5.2.1.0^2,6]dec-4-en-4-yl)-ethyl ester(206438-96-2)

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: 206438-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 206438-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,4,3 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 206438-96:
(8*2)+(7*0)+(6*6)+(5*4)+(4*3)+(3*8)+(2*9)+(1*6)=132
132 % 10 = 2
So 206438-96-2 is a valid CAS Registry Number.

206438-96-2Upstream product

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206438-96-2Relevant academic research and scientific papers

Stereoselective hetero-claisen rearrangement of camphor derived oxazoline-N-oxides

Dalko, Peter I.,Langlois, Yves

, p. 2107 - 2110 (2007/10/03)

Camphor derived oxazoline-N-oxides in the presence of various acylating agents afforded α-acyloxyoxazolines resulting from a diastereoselective [3,3] rearrangement. The configuration of the newly formed asymmetric center was established by chemical correlation. The observed diastereoselectivity accounts a concerted rather than a stepwise process.

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