Cas 905711-33-3,((2R,4S,6R)-2-Benzyloxymethyl-6-undecyl-tetrahydro-pyran-4-yloxy)-tert-butyl-dimethyl-silane

905711-33-3

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Basic information

Product Name: ((2R,4S,6R)-2-Benzyloxymethyl-6-undecyl-tetrahydro-pyran-4-yloxy)-tert-butyl-dimethyl-silane
Synonyms: ((2R,4S,6R)-2-Benzyloxymethyl-6-undecyl-tetrahydro-pyran-4-yloxy)-tert-butyl-dimethyl-silane
CAS NO:905711-33-3
Molecular Formula:
Molecular Weight: 490.842
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,4S,6R)-2-Benzyloxymethyl-6-undecyl-tetrahydro-pyran-4-yloxy)-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,4S,6R)-2-Benzyloxymethyl-6-undecyl-tetrahydro-pyran-4-yloxy)-tert-butyl-dimethyl-silane(905711-33-3)
EPA Substance Registry System: ((2R,4S,6R)-2-Benzyloxymethyl-6-undecyl-tetrahydro-pyran-4-yloxy)-tert-butyl-dimethyl-silane(905711-33-3)

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: 905711-33-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 905711-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,7,1 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 905711-33:
(8*9)+(7*0)+(6*5)+(5*7)+(4*1)+(3*1)+(2*3)+(1*3)=153
153 % 10 = 3
So 905711-33-3 is a valid CAS Registry Number.

905711-33-3Upstream product

905711-33-3Downstream Products

905711-33-3Relevant academic research and scientific papers

Stereoselective syntheses of (-)-tetrahydrolipstatin via Prins cyclisations

Yadav,Reddy, M. Sridhar,Prasad

, p. 4995 - 4998 (2007/10/03)

Stereoselective syntheses of (-)-tetrahydrolipstatin have been achieved via two divergent approaches through Prins cyclisations as the key steps. PCC mediated oxidative cleavage, Frater alkylation, Keck allylation, Sharpless asymmetric epoxidation and allylic cleavage were the other key steps employed.

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