Cas 120417-93-8,<3aR(3aα,5β,6β,6aα)>-tetrahydro-2,2-dimethyl-5-(2-oxopropyl)-6-(phenylmethoxy)furo<2,3-d>-1,3-dioxole

120417-93-8

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Basic information

Product Name: <3aR(3aα,5β,6β,6aα)>-tetrahydro-2,2-dimethyl-5-(2-oxopropyl)-6-(phenylmethoxy)furo<2,3-d>-1,3-dioxole
Synonyms:
CAS NO:120417-93-8
Molecular Formula:
Molecular Weight: 306.359
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: <3aR(3aα,5β,6β,6aα)>-tetrahydro-2,2-dimethyl-5-(2-oxopropyl)-6-(phenylmethoxy)furo<2,3-d>-1,3-dioxole(CAS DataBase Reference)
NIST Chemistry Reference: <3aR(3aα,5β,6β,6aα)>-tetrahydro-2,2-dimethyl-5-(2-oxopropyl)-6-(phenylmethoxy)furo<2,3-d>-1,3-dioxole(120417-93-8)
EPA Substance Registry System: <3aR(3aα,5β,6β,6aα)>-tetrahydro-2,2-dimethyl-5-(2-oxopropyl)-6-(phenylmethoxy)furo<2,3-d>-1,3-dioxole(120417-93-8)

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: 120417-93-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120417-93-8 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 120417-93:
(8*1)+(7*2)+(6*0)+(5*4)+(4*1)+(3*7)+(2*9)+(1*3)=88
88 % 10 = 8
So 120417-93-8 is a valid CAS Registry Number.

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120417-93-8Relevant 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 (1989)

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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