Cas 869809-01-8,(3R,3aS,8aS,8bR,S<sub>S</sub>)-3-ethoxy-8b-[(4-methylphenyl)sulfinyl]-3a,6,7,8,8a,8b-hexahydrofuro[3,4-d]pyrrolo[1,2-b]isoxazol-1(3H)-one

869809-01-8

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Basic information

Product Name: (3R,3aS,8aS,8bR,S_S)-3-ethoxy-8b-[(4-methylphenyl)sulfinyl]-3a,6,7,8,8a,8b-hexahydrofuro[3,4-d]pyrrolo[1,2-b]isoxazol-1(3H)-one
Synonyms: (3R,3aS,8aS,8bR,S_S)-3-ethoxy-8b-[(4-methylphenyl)sulfinyl]-3a,6,7,8,8a,8b-hexahydrofuro[3,4-d]pyrrolo[1,2-b]isoxazol-1(3H)-one
CAS NO:869809-01-8
Molecular Formula:
Molecular Weight: 351.423
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: (3R,3aS,8aS,8bR,S_S)-3-ethoxy-8b-[(4-methylphenyl)sulfinyl]-3a,6,7,8,8a,8b-hexahydrofuro[3,4-d]pyrrolo[1,2-b]isoxazol-1(3H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,3aS,8aS,8bR,S_S)-3-ethoxy-8b-[(4-methylphenyl)sulfinyl]-3a,6,7,8,8a,8b-hexahydrofuro[3,4-d]pyrrolo[1,2-b]isoxazol-1(3H)-one(869809-01-8)
EPA Substance Registry System: (3R,3aS,8aS,8bR,S_S)-3-ethoxy-8b-[(4-methylphenyl)sulfinyl]-3a,6,7,8,8a,8b-hexahydrofuro[3,4-d]pyrrolo[1,2-b]isoxazol-1(3H)-one(869809-01-8)

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: 869809-01-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 869809-01-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,9,8,0 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 869809-01:
(8*8)+(7*6)+(6*9)+(5*8)+(4*0)+(3*9)+(2*0)+(1*1)=228
228 % 10 = 8
So 869809-01-8 is a valid CAS Registry Number.

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869809-01-8Relevant academic research and scientific papers

The role of the sulfinyl group on the course of the reactions of 3-p-tolylsulfinylfuran-2(5H)-ones with nitrones. Synthetic uses of cycloreversion processes

Garcia Ruano, Jose L.,Fraile, Alberto,Martin Castro, Ana M.,Martin, M. Rosario

, p. 8825 - 8834 (2007/10/03)

The reaction of enantiopure 3-p-tolylsulfinylfuran-2(5H)-ones (2a and 2b) with cyclic (4) and acyclic (6) nitrones afforded furoisoxazolidines (5 and 7) in high yields under mild conditions. The reactivity of the dipolarophile was dramatically enhanced by

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