Cas 246859-64-3,<(2R,4R)-6-methoxy-4-(4-methoxybenzyl)-oxy-tetrahydropyran-2-yl>-acetic acid methyl ester

246859-64-3

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Basic information

Product Name: <(2R,4R)-6-methoxy-4-(4-methoxybenzyl)-oxy-tetrahydropyran-2-yl>-acetic acid methyl ester
Synonyms: <(2R,4R)-6-methoxy-4-(4-methoxybenzyl)-oxy-tetrahydropyran-2-yl>-acetic acid methyl ester
CAS NO:246859-64-3
Molecular Formula:
Molecular Weight: 324.374
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: <(2R,4R)-6-methoxy-4-(4-methoxybenzyl)-oxy-tetrahydropyran-2-yl>-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: <(2R,4R)-6-methoxy-4-(4-methoxybenzyl)-oxy-tetrahydropyran-2-yl>-acetic acid methyl ester(246859-64-3)
EPA Substance Registry System: <(2R,4R)-6-methoxy-4-(4-methoxybenzyl)-oxy-tetrahydropyran-2-yl>-acetic acid methyl ester(246859-64-3)

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: 246859-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 246859-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,6,8,5 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 246859-64:
(8*2)+(7*4)+(6*6)+(5*8)+(4*5)+(3*9)+(2*6)+(1*4)=183
183 % 10 = 3
So 246859-64-3 is a valid CAS Registry Number.

246859-64-3Upstream product

246859-64-3Downstream Products

1027592-68-2 2-[(2S,4R)-6-Methoxy-4-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-yl]-ethanol

246859-64-3Relevant academic research and scientific papers

Versatile 8-oxabicyclo[3.2.1]oct-6-en-3-one: stereoselective methodology for generating C-glycosides, delta-valerolactones, and polyacetate segments.

Vakalopoulos,Hoffmann

, p. 177 - 180 (2007/10/03)

[figure: see text] A new rearrangement of functionalized methoxy glycosides and a regioselective as well as stereoselective intramolecular Michael addition giving delta-valerolactones and C-glycosides are described. Applications to the synthesis of marine

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