Cas 183480-73-1,(2-Methoxy-phenyl)-[(R)-1-((S)-1-phenyl-ethyl)-aziridin-2-yl]-methanone

183480-73-1

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Basic information

Product Name: (2-Methoxy-phenyl)-[(R)-1-((S)-1-phenyl-ethyl)-aziridin-2-yl]-methanone
Synonyms: (2-Methoxy-phenyl)-[(R)-1-((S)-1-phenyl-ethyl)-aziridin-2-yl]-methanone
CAS NO:183480-73-1
Molecular Formula:
Molecular Weight: 281.354
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-Methoxy-phenyl)-[(R)-1-((S)-1-phenyl-ethyl)-aziridin-2-yl]-methanone(CAS DataBase Reference)
NIST Chemistry Reference: (2-Methoxy-phenyl)-[(R)-1-((S)-1-phenyl-ethyl)-aziridin-2-yl]-methanone(183480-73-1)
EPA Substance Registry System: (2-Methoxy-phenyl)-[(R)-1-((S)-1-phenyl-ethyl)-aziridin-2-yl]-methanone(183480-73-1)

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: 183480-73-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183480-73-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,4,8 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 183480-73:
(8*1)+(7*8)+(6*3)+(5*4)+(4*8)+(3*0)+(2*7)+(1*3)=151
151 % 10 = 1
So 183480-73-1 is a valid CAS Registry Number.

183480-73-1Upstream product

183480-73-1Downstream Products

183480-65-1 (R)-(2-Methoxy-phenyl)-[(R)-1-((S)-1-phenyl-ethyl)-aziridin-2-yl]-methanol

183480-73-1Relevant academic research and scientific papers

Highly diastereoselective reduction of enantiomerically pure aziridino ketones

Kim, Bong Chan,Lee, Won Koo

, p. 12117 - 12124 (1996)

Various enantiomerically pure aziridino ketones were prepared from the corresponding secondary alcohols by Swern oxidation. Those configurationally stable α-amino ketones were stereoselectively reduced by L-Selectride to provide the corresponding alcohol with high diastereoselectivities and chemical yields.

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