Cas 139192-60-2,(S)-2-[(2S,4S)-4-Isopropyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone

139192-60-2

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Basic information

Product Name: (S)-2-[(2S,4S)-4-Isopropyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone
Synonyms: (S)-2-[(2S,4S)-4-Isopropyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone
CAS NO:139192-60-2
Molecular Formula:
Molecular Weight: 365.494
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: (S)-2-[(2S,4S)-4-Isopropyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-[(2S,4S)-4-Isopropyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone(139192-60-2)
EPA Substance Registry System: (S)-2-[(2S,4S)-4-Isopropyl-3-(toluene-4-sulfonyl)-oxazolidin-2-yl]-cyclohexanone(139192-60-2)

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: 139192-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 139192-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,1,9 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139192-60:
(8*1)+(7*3)+(6*9)+(5*1)+(4*9)+(3*2)+(2*6)+(1*0)=142
142 % 10 = 2
So 139192-60-2 is a valid CAS Registry Number.

139192-60-2Upstream product

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139192-60-2Relevant academic research and scientific papers

Diastereoselective synthesis of enantiomerically pure 3-organosulfonyl-2-(2-oxocycloalkyl)-1,3-oxazolidines from 2-formylcycloalkanones and β-aminoalkanols

Hoppe,Hoffmann,Gartner,Krettek,Hoppe

, p. 1157 - 1162 (2007/10/02)

The title compounds (3-arylsulfonyl- or 3-mesyl-2-(2-oxocycloalkyl)-1,3-oxazolidines) belonging to two different diastereomeric series, are prepared selectively by variation of the condensation conditions. By this, the chiral information of the 2-amino-1-

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