Cas 1224893-06-4,(Z)-ethyl 2-(((2R,3S,5R,6S)-5-(benzyloxy)-6-(benzyloxymethyl)-3-(tert-butyldimethylsilyloxy)-6-methyltetrahydro-2H-pyran-2-yl)methylene)-3-methylbutanoate

1224893-06-4

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Basic information

Product Name: (Z)-ethyl 2-(((2R,3S,5R,6S)-5-(benzyloxy)-6-(benzyloxymethyl)-3-(tert-butyldimethylsilyloxy)-6-methyltetrahydro-2H-pyran-2-yl)methylene)-3-methylbutanoate
Synonyms: (Z)-ethyl 2-(((2R,3S,5R,6S)-5-(benzyloxy)-6-(benzyloxymethyl)-3-(tert-butyldimethylsilyloxy)-6-methyltetrahydro-2H-pyran-2-yl)methylene)-3-methylbutanoate
CAS NO:1224893-06-4
Molecular Formula:
Molecular Weight: 596.88
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: (Z)-ethyl 2-(((2R,3S,5R,6S)-5-(benzyloxy)-6-(benzyloxymethyl)-3-(tert-butyldimethylsilyloxy)-6-methyltetrahydro-2H-pyran-2-yl)methylene)-3-methylbutanoate(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-ethyl 2-(((2R,3S,5R,6S)-5-(benzyloxy)-6-(benzyloxymethyl)-3-(tert-butyldimethylsilyloxy)-6-methyltetrahydro-2H-pyran-2-yl)methylene)-3-methylbutanoate(1224893-06-4)
EPA Substance Registry System: (Z)-ethyl 2-(((2R,3S,5R,6S)-5-(benzyloxy)-6-(benzyloxymethyl)-3-(tert-butyldimethylsilyloxy)-6-methyltetrahydro-2H-pyran-2-yl)methylene)-3-methylbutanoate(1224893-06-4)

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: 1224893-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1224893-06-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,8,9 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1224893-06:
(9*1)+(8*2)+(7*2)+(6*4)+(5*8)+(4*9)+(3*3)+(2*0)+(1*6)=154
154 % 10 = 4
So 1224893-06-4 is a valid CAS Registry Number.

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1224893-06-4Relevant academic research and scientific papers

Regio- and stereocontrol in rhenium-catalyzed transposition of allylic alcohols

Herrmann, Aaron T.,Saito, Tatsuo,Stivala, Craig E.,Tom, Janine,Zakarian, Armen

supporting information; experimental part, p. 5962 - 5963 (2010/07/05)

A hydroxyl group-directed, highly regio- and stereoselective transposition of allylic alcohols based on rhenium catalysis has been developed. The method is suitable for a direct isomerization of acetals into the thermodynamically preferred isomer as long as one of the hydroxyl groups is allylic. This method will expand the scope of rhenium-catalyzed alcohol transpositions for complex molecule synthesis.

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