Cas 928119-11-3,3-Cyclohexen-1-one, 2-[[(2S)-2-(methoxymethyl)-1-pyrrolidinyl]carbonyl]-4-(4-methoxyphenyl)- 2-(2-propen-1-yl)-, (2R)-

928119-11-3

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Basic information

Product Name: 3-Cyclohexen-1-one, 2-[[(2S)-2-(methoxymethyl)-1-pyrrolidinyl]carbonyl]-4-(4-methoxyphenyl)- 2-(2-propen-1-yl)-, (2R)-
Synonyms:
CAS NO:928119-11-3
Molecular Formula: C23H29NO4
Molecular Weight: 383.488
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: 3-Cyclohexen-1-one, 2-[[(2S)-2-(methoxymethyl)-1-pyrrolidinyl]carbonyl]-4-(4-methoxyphenyl)- 2-(2-propen-1-yl)-, (2R)-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Cyclohexen-1-one, 2-[[(2S)-2-(methoxymethyl)-1-pyrrolidinyl]carbonyl]-4-(4-methoxyphenyl)- 2-(2-propen-1-yl)-, (2R)-(928119-11-3)
EPA Substance Registry System: 3-Cyclohexen-1-one, 2-[[(2S)-2-(methoxymethyl)-1-pyrrolidinyl]carbonyl]-4-(4-methoxyphenyl)- 2-(2-propen-1-yl)-, (2R)-(928119-11-3)

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: 928119-11-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 928119-11-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,1,1 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 928119-11:
(8*9)+(7*2)+(6*8)+(5*1)+(4*1)+(3*9)+(2*1)+(1*1)=173
173 % 10 = 3
So 928119-11-3 is a valid CAS Registry Number.

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928119-11-3Relevant academic research and scientific papers

Exploration of the enantioselective Birch-Cope sequence for the synthesis of carbocyclic quaternary stereocenters

Paul, Tapas,Malachowski, William P.,Lee, Jisun

, p. 930 - 937 (2007/10/03)

(Chemical Equation Presented) Quaternary stereocenters on a 2-cyclohexen-1-one ring are synthesized with good to excellent levels of enantioselectivity. The quaternary stereocenter is created through a new synthetic sequence involving three reactions: the

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