Cas 1369963-75-6,(2R,3aS,4S,5S)-4,5-bis(benzyloxy)-2-phenylsulfonyl-hexahydropyrrolo[1,2-b]isoxazole

1369963-75-6

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Basic information

Product Name: (2R,3aS,4S,5S)-4,5-bis(benzyloxy)-2-phenylsulfonyl-hexahydropyrrolo[1,2-b]isoxazole
Synonyms: (2R,3aS,4S,5S)-4,5-bis(benzyloxy)-2-phenylsulfonyl-hexahydropyrrolo[1,2-b]isoxazole
CAS NO:1369963-75-6
Molecular Formula:
Molecular Weight: 465.57
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: (2R,3aS,4S,5S)-4,5-bis(benzyloxy)-2-phenylsulfonyl-hexahydropyrrolo[1,2-b]isoxazole(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3aS,4S,5S)-4,5-bis(benzyloxy)-2-phenylsulfonyl-hexahydropyrrolo[1,2-b]isoxazole(1369963-75-6)
EPA Substance Registry System: (2R,3aS,4S,5S)-4,5-bis(benzyloxy)-2-phenylsulfonyl-hexahydropyrrolo[1,2-b]isoxazole(1369963-75-6)

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: 1369963-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1369963-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,9,6 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1369963-75:
(9*1)+(8*3)+(7*6)+(6*9)+(5*9)+(4*6)+(3*3)+(2*7)+(1*5)=226
226 % 10 = 6
So 1369963-75-6 is a valid CAS Registry Number.

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1369963-75-6Relevant academic research and scientific papers

1,3-Dipolar cycloaddition of nitrones with phenylvinyl sulfone. An experimental and theoretical study

Flores, Marife,Garcia, Pilar,Garrido, Narciso M.,Nieto, Carlos T.,Basabe, Pilar,Marcos, Isidro S.,Sanz-Gonzalez, Francisca,Goodman, Jonathan M.,Diez, David

experimental part, p. 76 - 85 (2012/05/20)

The addition of three nitrones to phenylvinylsulfone, 1, has been studied. The stereochemistry previously established by two-dimensional NMR techniques was confirmed by X-ray crystal structure determination. Theoretical studies made us propose that this r

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