Cas 120417-95-0,2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-phenyl-ethanone

120417-95-0

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Basic information

Product Name: 2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-phenyl-ethanone
Synonyms: 2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-phenyl-ethanone
CAS NO:120417-95-0
Molecular Formula:
Molecular Weight: 368.43
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-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-phenyl-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-phenyl-ethanone(120417-95-0)
EPA Substance Registry System: 2-((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-1-phenyl-ethanone(120417-95-0)

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: 120417-95-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120417-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,1 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120417-95:
(8*1)+(7*2)+(6*0)+(5*4)+(4*1)+(3*7)+(2*9)+(1*5)=90
90 % 10 = 0
So 120417-95-0 is a valid CAS Registry Number.

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120417-95-0Relevant academic research and scientific papers

New Chirons from D-Glucose. Regio- and Diastereoselective C-C Bond Forming Reactions Exploiting Novel Aldotetrafuranose Acetates as Chiral Synthetic Equivalents of Tartaric Aldehydes

Dhavale, Dilip D.,Tagliavini, Emilio,Trombini, Claudio,Umani-Ronchi, Achille

, p. 4100 - 4105 (2007/10/02)

Two differentially protected tetrafuranose acetates 5 and 6 have been prepared from diacetone D-glucose in parallel short routes.They clearly act as chiral synthetic equivalents of D- and meso-tartaric aldehydes when exploited in Lewis acid promoted react

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