Cas 942598-47-2,(3aS,4R,11S,11aR)-4-methyl-11-((R)-N-methyl-S-phenylsulfonimidoyl)-2,3,3a,4,8,9,10,11-octahydrocyclopenta[d]pyrido[1,2-c][1,3]oxazin-6(1H)-one

942598-47-2

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Basic information

Product Name: (3aS,4R,11S,11aR)-4-methyl-11-((R)-N-methyl-S-phenylsulfonimidoyl)-2,3,3a,4,8,9,10,11-octahydrocyclopenta[d]pyrido[1,2-c][1,3]oxazin-6(1H)-one
Synonyms: (3aS,4R,11S,11aR)-4-methyl-11-((R)-N-methyl-S-phenylsulfonimidoyl)-2,3,3a,4,8,9,10,11-octahydrocyclopenta[d]pyrido[1,2-c][1,3]oxazin-6(1H)-one
CAS NO:942598-47-2
Molecular Formula:
Molecular Weight: 362.493
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: (3aS,4R,11S,11aR)-4-methyl-11-((R)-N-methyl-S-phenylsulfonimidoyl)-2,3,3a,4,8,9,10,11-octahydrocyclopenta[d]pyrido[1,2-c][1,3]oxazin-6(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,11S,11aR)-4-methyl-11-((R)-N-methyl-S-phenylsulfonimidoyl)-2,3,3a,4,8,9,10,11-octahydrocyclopenta[d]pyrido[1,2-c][1,3]oxazin-6(1H)-one(942598-47-2)
EPA Substance Registry System: (3aS,4R,11S,11aR)-4-methyl-11-((R)-N-methyl-S-phenylsulfonimidoyl)-2,3,3a,4,8,9,10,11-octahydrocyclopenta[d]pyrido[1,2-c][1,3]oxazin-6(1H)-one(942598-47-2)

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: 942598-47-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 942598-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,2,5,9 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 942598-47:
(8*9)+(7*4)+(6*2)+(5*5)+(4*9)+(3*8)+(2*4)+(1*7)=212
212 % 10 = 2
So 942598-47-2 is a valid CAS Registry Number.

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942598-47-2Relevant academic research and scientific papers

Modular asymmetric synthesis of functionalized azaspirocycles based on the sulfoximine auxiliary

Adrien, Adeline,Gais, Hans-Joachim,Koehler, Franz,Runsink, Jan,Raabe, Gerhard

, p. 2155 - 2158 (2008/02/03)

A modular asymmetric synthesis of the functionalized azaspirocycles 6 (m = 2, n = 1), 7 (m = 1, n = 2), 8 (m = n = 2), 12, 20, and 24 from the cyclic allylic sulfoximines 1 is described. The synthetic strategy is based on the stereoselective construction

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