Cas 958265-83-3,2-hydroxyethyl (1R,3S,4R,5S,6R)-1-azidomethyl-5,6-dibenzyloxy-2,7-dioxabicyclo[2.2.1]heptane-3-carboxylate

958265-83-3

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Basic information

Product Name: 2-hydroxyethyl (1R,3S,4R,5S,6R)-1-azidomethyl-5,6-dibenzyloxy-2,7-dioxabicyclo[2.2.1]heptane-3-carboxylate
Synonyms: 2-hydroxyethyl (1R,3S,4R,5S,6R)-1-azidomethyl-5,6-dibenzyloxy-2,7-dioxabicyclo[2.2.1]heptane-3-carboxylate
CAS NO:958265-83-3
Molecular Formula:
Molecular Weight: 455.467
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: 2-hydroxyethyl (1R,3S,4R,5S,6R)-1-azidomethyl-5,6-dibenzyloxy-2,7-dioxabicyclo[2.2.1]heptane-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: 2-hydroxyethyl (1R,3S,4R,5S,6R)-1-azidomethyl-5,6-dibenzyloxy-2,7-dioxabicyclo[2.2.1]heptane-3-carboxylate(958265-83-3)
EPA Substance Registry System: 2-hydroxyethyl (1R,3S,4R,5S,6R)-1-azidomethyl-5,6-dibenzyloxy-2,7-dioxabicyclo[2.2.1]heptane-3-carboxylate(958265-83-3)

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: 958265-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 958265-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,2,6 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 958265-83:
(8*9)+(7*5)+(6*8)+(5*2)+(4*6)+(3*5)+(2*8)+(1*3)=223
223 % 10 = 3
So 958265-83-3 is a valid CAS Registry Number.

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958265-83-3Relevant academic research and scientific papers

Synthetic routes to three novel scaffolds for potential glycosidase inhibitors

Rommel, Michael,Ernst, Alexander,Koert, Ulrich

, p. 4408 - 4430 (2008/09/17)

Efficient syntheses of three novel scaffolds for potential β-glycosidase inhibitors were developed: The first consists of a 2,7-dioxabicyclo[2.2.1]heptane derivative, which was prepared by an intramolecular ketalisation. The second scaffold consists of a

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