Cas 108739-79-3,((4R,5S,6R)-2-Benzenesulfinyl-4,5-bis-benzyloxy-6-benzyloxymethyl-5,6-dihydro-4H-pyran-3-yl)-phenyl-methanol

108739-79-3

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Basic information

Product Name: ((4R,5S,6R)-2-Benzenesulfinyl-4,5-bis-benzyloxy-6-benzyloxymethyl-5,6-dihydro-4H-pyran-3-yl)-phenyl-methanol
Synonyms:
CAS NO:108739-79-3
Molecular Formula:
Molecular Weight: 646.804
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: ((4R,5S,6R)-2-Benzenesulfinyl-4,5-bis-benzyloxy-6-benzyloxymethyl-5,6-dihydro-4H-pyran-3-yl)-phenyl-methanol(CAS DataBase Reference)
NIST Chemistry Reference: ((4R,5S,6R)-2-Benzenesulfinyl-4,5-bis-benzyloxy-6-benzyloxymethyl-5,6-dihydro-4H-pyran-3-yl)-phenyl-methanol(108739-79-3)
EPA Substance Registry System: ((4R,5S,6R)-2-Benzenesulfinyl-4,5-bis-benzyloxy-6-benzyloxymethyl-5,6-dihydro-4H-pyran-3-yl)-phenyl-methanol(108739-79-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 108739-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 108739-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,3 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108739-79:
(8*1)+(7*0)+(6*8)+(5*7)+(4*3)+(3*9)+(2*7)+(1*9)=153
153 % 10 = 3
So 108739-79-3 is a valid CAS Registry Number.

108739-79-3Upstream product

108739-79-3Downstream Products

108739-79-3Relevant academic research and scientific papers

DIRECT LITHIATION OF GLYCALS. SYNTHESIS OF C-2 BRANCHED SUGARS

Schmidt, Richard R,,Kast, Juergen

, p. 4007 - 4010 (1986)

Direct lithiation at the C-2 atom of 1-phenylsulfinyl substituted glucals 4a,b can be readily performed with LDA as indicated by reactions of different C-electrophiles.Ohenylsulfinyl group removal takes place in the aldehyde reaction products by simple th

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