Cas 115494-17-2,benzyl 5-O-benzyl-2-deoxy-3-O-<(2-methylsulfonyl)ethyl>-α-D-erythro-pentofuranosylacetate

115494-17-2

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Basic information

Product Name: benzyl 5-O-benzyl-2-deoxy-3-O-<(2-methylsulfonyl)ethyl>-α-D-erythro-pentofuranosylacetate
Synonyms:
CAS NO:115494-17-2
Molecular Formula:
Molecular Weight: 462.564
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: benzyl 5-O-benzyl-2-deoxy-3-O-<(2-methylsulfonyl)ethyl>-α-D-erythro-pentofuranosylacetate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 5-O-benzyl-2-deoxy-3-O-<(2-methylsulfonyl)ethyl>-α-D-erythro-pentofuranosylacetate(115494-17-2)
EPA Substance Registry System: benzyl 5-O-benzyl-2-deoxy-3-O-<(2-methylsulfonyl)ethyl>-α-D-erythro-pentofuranosylacetate(115494-17-2)

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: 115494-17-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115494-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,4,9 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 115494-17:
(8*1)+(7*1)+(6*5)+(5*4)+(4*9)+(3*4)+(2*1)+(1*7)=122
122 % 10 = 2
So 115494-17-2 is a valid CAS Registry Number.

115494-17-2Upstream product

115494-17-2Downstream Products

115494-17-2Relevant academic research and scientific papers

Stereoselective Preparation of β-C-Glycosides from 2-Deoxyribose Utilizing Neighboring Participation by 3-O-Methylsulfinylethyl Group

Narasaka, Koichi,Ichikawa, Yuh-ichiro,Kubota, Hideki

, p. 2139 - 2142 (1987)

Acid catalyzed reaction of 2-deoxy-3-O-methylsulfinylethylribofuranosyl acetate with silyl enol ethers proceeded stereoselectively, resulting in the predominant formation of the corresponding β-C-glycosides.

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