Cas 900502-97-8,(2R,3R,3aS,5R,6aR)-3-Benzyloxy-2-benzyloxymethyl-5-methyl-hexahydro-furo[3,2-b]furan

900502-97-8

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Basic information

Product Name: (2R,3R,3aS,5R,6aR)-3-Benzyloxy-2-benzyloxymethyl-5-methyl-hexahydro-furo[3,2-b]furan
Synonyms: (2R,3R,3aS,5R,6aR)-3-Benzyloxy-2-benzyloxymethyl-5-methyl-hexahydro-furo[3,2-b]furan
CAS NO:900502-97-8
Molecular Formula:
Molecular Weight: 354.446
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: (2R,3R,3aS,5R,6aR)-3-Benzyloxy-2-benzyloxymethyl-5-methyl-hexahydro-furo[3,2-b]furan(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,3aS,5R,6aR)-3-Benzyloxy-2-benzyloxymethyl-5-methyl-hexahydro-furo[3,2-b]furan(900502-97-8)
EPA Substance Registry System: (2R,3R,3aS,5R,6aR)-3-Benzyloxy-2-benzyloxymethyl-5-methyl-hexahydro-furo[3,2-b]furan(900502-97-8)

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: 900502-97-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 900502-97-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,0,5,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 900502-97:
(8*9)+(7*0)+(6*0)+(5*5)+(4*0)+(3*2)+(2*9)+(1*7)=128
128 % 10 = 8
So 900502-97-8 is a valid CAS Registry Number.

900502-97-8Upstream product

93836-22-7 4,7-anhydro-5,6,8-tri-O-benzyl-1,2,3-trideoxy-D-altro-oct-1-enitol

900502-97-8Downstream Products

900502-97-8Relevant academic research and scientific papers

Stereoselective synthesis of dioxabicycles from 1-C-allyl-2-O-benzyl- glycosides - An intramolecular cyclization between 2-O-benzyl oxygen and the allyl double bond

Wu, An-Tai,Yi, Tian,Shao, Huawu,Wu, Shih-Hsiung,Zou, Wei

, p. 597 - 602 (2006)

Addition of a proton to the double bond of 1-C-allyl-O-benzylglycosides gave a 2′-carbonium ion, which in turn reacted intramolecularly, in a regio- and diastereo-selective manner, with the nucleophilic oxygen of the 2-O-benzyl group to form an oxonium in

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