Cas 132573-06-9,(2S,6S)-2-((S)-1-Hydroxy-2-methyl-propyl)-6-[(2R,4R)-4-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone

132573-06-9

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Basic information

Product Name: (2S,6S)-2-((S)-1-Hydroxy-2-methyl-propyl)-6-[(2R,4R)-4-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone
Synonyms: (2S,6S)-2-((S)-1-Hydroxy-2-methyl-propyl)-6-[(2R,4R)-4-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone
CAS NO:132573-06-9
Molecular Formula:
Molecular Weight: 471.618
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: (2S,6S)-2-((S)-1-Hydroxy-2-methyl-propyl)-6-[(2R,4R)-4-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone(CAS DataBase Reference)
NIST Chemistry Reference: (2S,6S)-2-((S)-1-Hydroxy-2-methyl-propyl)-6-[(2R,4R)-4-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone(132573-06-9)
EPA Substance Registry System: (2S,6S)-2-((S)-1-Hydroxy-2-methyl-propyl)-6-[(2R,4R)-4-phenyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone(132573-06-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 132573-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132573-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,7 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 132573-06:
(8*1)+(7*3)+(6*2)+(5*5)+(4*7)+(3*3)+(2*0)+(1*6)=109
109 % 10 = 9
So 132573-06-9 is a valid CAS Registry Number.

132573-06-9Upstream product

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132573-06-9Relevant academic research and scientific papers

ASYMMETRIC ALDOL ADDITION REACTIONS OF A CHIRAL 3-SULFONYL-1,3-OXAZOLIDINE-MASKED LITHIUM 2-FORMYLCYCLOHEXANONE ENOLATE

Hoppe, Inga,Hoppe, Dieter,Herbst-Irmer, Regine,Egert, Ernst

, p. 6859 - 6862 (1990)

The title compound, prepared by kinetically controlled deprotonation of a stereohomogeneous 2-(2-oxocyclohexyl)-1,3-oxazolidine, undergoes highly anti-stereoselective aldol addition with alkanals.

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