Cas 172473-56-2,(3aR,6S,6aS,3'aR,6'S,6'aS)-1,1'-Bis-(4-methoxy-benzyl)-octahydro-[6,6']bi[furo[3,4-c]isoxazolyl]

172473-56-2

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Basic information

Product Name: (3aR,6S,6aS,3'aR,6'S,6'aS)-1,1'-Bis-(4-methoxy-benzyl)-octahydro-[6,6']bi[furo[3,4-c]isoxazolyl]
Synonyms: (3aR,6S,6aS,3'aR,6'S,6'aS)-1,1'-Bis-(4-methoxy-benzyl)-octahydro-[6,6']bi[furo[3,4-c]isoxazolyl]
CAS NO:172473-56-2
Molecular Formula:
Molecular Weight: 468.55
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: (3aR,6S,6aS,3'aR,6'S,6'aS)-1,1'-Bis-(4-methoxy-benzyl)-octahydro-[6,6']bi[furo[3,4-c]isoxazolyl](CAS DataBase Reference)
NIST Chemistry Reference: (3aR,6S,6aS,3'aR,6'S,6'aS)-1,1'-Bis-(4-methoxy-benzyl)-octahydro-[6,6']bi[furo[3,4-c]isoxazolyl](172473-56-2)
EPA Substance Registry System: (3aR,6S,6aS,3'aR,6'S,6'aS)-1,1'-Bis-(4-methoxy-benzyl)-octahydro-[6,6']bi[furo[3,4-c]isoxazolyl](172473-56-2)

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: 172473-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 172473-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,4,7 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 172473-56:
(8*1)+(7*7)+(6*2)+(5*4)+(4*7)+(3*3)+(2*5)+(1*6)=142
142 % 10 = 2
So 172473-56-2 is a valid CAS Registry Number.

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172473-56-2Relevant academic research and scientific papers

Intramolecular 1,3-dipolar cycloaddition of transient enantiomerically pure oxaalkenyl nitrones

Aurich,Biesemeier

, p. 1171 - 1178 (1995)

A variety of enantiomerically pure α-hydroxy esters were converted into enantiomerically pure 3,7-dioxa-2-azabicyclo[3.3.0]octanes 7 by the following reaction sequence. A1lylation of the hydroxy group was followed by reduction of the ester group. The resu

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