Cas 1392201-60-3,N-((1R,2S,3R,4S)-6-(tert-butyldimethylsilyloxy)-3-(3-chlorophenyl)-5-(2-hydroxyethyl)-2-(hydroxymethyl)bicyclo[2.2.2]oct-5-en-2-yl)benzamide

1392201-60-3

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Basic information

Product Name: N-((1R,2S,3R,4S)-6-(tert-butyldimethylsilyloxy)-3-(3-chlorophenyl)-5-(2-hydroxyethyl)-2-(hydroxymethyl)bicyclo[2.2.2]oct-5-en-2-yl)benzamide
Synonyms: N-((1R,2S,3R,4S)-6-(tert-butyldimethylsilyloxy)-3-(3-chlorophenyl)-5-(2-hydroxyethyl)-2-(hydroxymethyl)bicyclo[2.2.2]oct-5-en-2-yl)benzamide
CAS NO:1392201-60-3
Molecular Formula:
Molecular Weight: 542.19
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: N-((1R,2S,3R,4S)-6-(tert-butyldimethylsilyloxy)-3-(3-chlorophenyl)-5-(2-hydroxyethyl)-2-(hydroxymethyl)bicyclo[2.2.2]oct-5-en-2-yl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((1R,2S,3R,4S)-6-(tert-butyldimethylsilyloxy)-3-(3-chlorophenyl)-5-(2-hydroxyethyl)-2-(hydroxymethyl)bicyclo[2.2.2]oct-5-en-2-yl)benzamide(1392201-60-3)
EPA Substance Registry System: N-((1R,2S,3R,4S)-6-(tert-butyldimethylsilyloxy)-3-(3-chlorophenyl)-5-(2-hydroxyethyl)-2-(hydroxymethyl)bicyclo[2.2.2]oct-5-en-2-yl)benzamide(1392201-60-3)

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: 1392201-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1392201-60-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,2,0 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1392201-60:
(9*1)+(8*3)+(7*9)+(6*2)+(5*2)+(4*0)+(3*1)+(2*6)+(1*0)=133
133 % 10 = 3
So 1392201-60-3 is a valid CAS Registry Number.

1392201-60-3Upstream product

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1392201-60-3Relevant academic research and scientific papers

Cross-trienamines in asymmetric organocatalysis

Halskov, Kim Soholm,Johansen, Tore Kiilerich,Davis, Rebecca L.,Steurer, Marianne,Jensen, Frank,Jorgensen, Karl Anker

supporting information; experimental part, p. 12943 - 12946 (2012/09/25)

Cross-conjugated trienamines are introduced as a new concept in asymmetric organocatalysis. These intermediates are applied in highly enantioselective Diels-Alder and addition reactions, providing functionalized bicyclo[2.2.2]octane compounds and γ′-addition products, respectively. The nature of the transformations and the intermediates involved are investigated by computational calculations and NMR analysis.

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