Cas 198060-26-3,1-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-prop-2-en-1-ol

198060-26-3

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Basic information

Product Name: 1-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-prop-2-en-1-ol
Synonyms: 1-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-prop-2-en-1-ol
CAS NO:198060-26-3
Molecular Formula:
Molecular Weight: 580.721
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: 1-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-prop-2-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: 1-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-prop-2-en-1-ol(198060-26-3)
EPA Substance Registry System: 1-((2S,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-prop-2-en-1-ol(198060-26-3)

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: 198060-26-3(Hazardous Substances Data)

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198060-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198060-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,0,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 198060-26:
(8*1)+(7*9)+(6*8)+(5*0)+(4*6)+(3*0)+(2*2)+(1*6)=153
153 % 10 = 3
So 198060-26-3 is a valid CAS Registry Number.

198060-26-3Upstream product

113019-43-5 2,3,4,6-tetra-O-benzyl-1-formyl-D-glucopyranose

198060-26-3Downstream Products

198060-26-3Relevant academic research and scientific papers

A Pd(0)-catalyzed route to functionalized β-C-glycosides from β-C glycosylaldehydes

Michelet, Veronique,Genet, Jean-Pierre,Dujardin, Gilles

, p. 7741 - 7744 (1997)

C-glycosides are synthesized in five steps starting from β-C- glycosylaldehydes 1 and 2. The key step is a Pd(0)-catalyzed alkylation that leads regio and stereoselectively to exotic compounds by formation of C-C and C-N bonds.

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