Cas 115828-13-2,(4aR,6R,7S,8R,8aR)-7,8-Diacetoxy-6-acetoxymethyl-3-benzyloxy-6,7,8,8a-tetrahydro-4aH-pyrano[3,2-e][1,3,4]oxadiazine-1-carboxylic acid benzyl ester

115828-13-2

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Basic information

Product Name: (4aR,6R,7S,8R,8aR)-7,8-Diacetoxy-6-acetoxymethyl-3-benzyloxy-6,7,8,8a-tetrahydro-4aH-pyrano[3,2-e][1,3,4]oxadiazine-1-carboxylic acid benzyl ester
Synonyms: (4aR,6R,7S,8R,8aR)-7,8-Diacetoxy-6-acetoxymethyl-3-benzyloxy-6,7,8,8a-tetrahydro-4aH-pyrano[3,2-e][1,3,4]oxadiazine-1-carboxylic acid benzyl ester
CAS NO:115828-13-2
Molecular Formula:
Molecular Weight: 570.553
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: (4aR,6R,7S,8R,8aR)-7,8-Diacetoxy-6-acetoxymethyl-3-benzyloxy-6,7,8,8a-tetrahydro-4aH-pyrano[3,2-e][1,3,4]oxadiazine-1-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,6R,7S,8R,8aR)-7,8-Diacetoxy-6-acetoxymethyl-3-benzyloxy-6,7,8,8a-tetrahydro-4aH-pyrano[3,2-e][1,3,4]oxadiazine-1-carboxylic acid benzyl ester(115828-13-2)
EPA Substance Registry System: (4aR,6R,7S,8R,8aR)-7,8-Diacetoxy-6-acetoxymethyl-3-benzyloxy-6,7,8,8a-tetrahydro-4aH-pyrano[3,2-e][1,3,4]oxadiazine-1-carboxylic acid benzyl ester(115828-13-2)

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: 115828-13-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115828-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,2 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115828-13:
(8*1)+(7*1)+(6*5)+(5*8)+(4*2)+(3*8)+(2*1)+(1*3)=122
122 % 10 = 2
So 115828-13-2 is a valid CAS Registry Number.

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115828-13-2Relevant academic research and scientific papers

Cycloaddition Reaction of Dibenzyl Azodicarboxylate and Glycals

Leblanc, Yves,Fitzsimmons, Brian J.,Springer, James P.,Rokach, Joshua

, p. 2995 - 3000 (2007/10/02)

The cycloaddition reaction of dibenzyl azodicarboxylate and glycals allows the stereoselective introduction of an amino function at C-2 of a carbohydrate.Very good results were obtained with both furanoid and pyranoid glycals, except when triacetylglucal (TAG) was used as the substrate.In some instances the course of the reaction was found to be concentration dependent.

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