Cas 528566-69-0,(1S,3R,4S,5S,6R,7R)-[6,7-bis(benzyloxy)-3-methoxy-2-oxabicyclo[2.2.1]hept-5-yl]carbamic acid benzyl ester

528566-69-0

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Basic information

Product Name: (1S,3R,4S,5S,6R,7R)-[6,7-bis(benzyloxy)-3-methoxy-2-oxabicyclo[2.2.1]hept-5-yl]carbamic acid benzyl ester
Synonyms: (1S,3R,4S,5S,6R,7R)-[6,7-bis(benzyloxy)-3-methoxy-2-oxabicyclo[2.2.1]hept-5-yl]carbamic acid benzyl ester
CAS NO:528566-69-0
Molecular Formula:
Molecular Weight: 489.568
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: (1S,3R,4S,5S,6R,7R)-[6,7-bis(benzyloxy)-3-methoxy-2-oxabicyclo[2.2.1]hept-5-yl]carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3R,4S,5S,6R,7R)-[6,7-bis(benzyloxy)-3-methoxy-2-oxabicyclo[2.2.1]hept-5-yl]carbamic acid benzyl ester(528566-69-0)
EPA Substance Registry System: (1S,3R,4S,5S,6R,7R)-[6,7-bis(benzyloxy)-3-methoxy-2-oxabicyclo[2.2.1]hept-5-yl]carbamic acid benzyl ester(528566-69-0)

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: 528566-69-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 528566-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,8,5,6 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 528566-69:
(8*5)+(7*2)+(6*8)+(5*5)+(4*6)+(3*6)+(2*6)+(1*9)=190
190 % 10 = 0
So 528566-69-0 is a valid CAS Registry Number.

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528566-69-0Relevant academic research and scientific papers

Stereocontrolled transformation of nitrohexofuranoses into cyclopentylamines via 2-oxabicyclo[2.2.1]heptanes: Incorporation of polyhydroxylated carbocyclic β-amino acids into peptides

Soengas, Raquel G.,Estevez, Juan C.,Estevez, Ramon J.

, p. 1423 - 1425 (2007/10/03)

(Matrix presented) A promising new strategy for the transformation of nitrohexofuranoses into cyclopentylamines, based on intramolecular cyclization followed by controlled opening of the resulting 2-oxabicyclo[2.2.1]heptane derivatives, allowed the first

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