Cas 116159-24-1,3-((2R,3R)-3-{2-[(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-oxiranyl]-ethyl}-3-methyl-oxiranyl)-propionaldehyde

116159-24-1

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Basic information

Product Name: 3-((2R,3R)-3-{2-[(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-oxiranyl]-ethyl}-3-methyl-oxiranyl)-propionaldehyde
Synonyms:
CAS NO:116159-24-1
Molecular Formula:
Molecular Weight: 466.693
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: 3-((2R,3R)-3-{2-[(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-oxiranyl]-ethyl}-3-methyl-oxiranyl)-propionaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 3-((2R,3R)-3-{2-[(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-oxiranyl]-ethyl}-3-methyl-oxiranyl)-propionaldehyde(116159-24-1)
EPA Substance Registry System: 3-((2R,3R)-3-{2-[(2R,3R)-3-(tert-Butyl-diphenyl-silanyloxymethyl)-3-methyl-oxiranyl]-ethyl}-3-methyl-oxiranyl)-propionaldehyde(116159-24-1)

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: 116159-24-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116159-24-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,5 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 116159-24:
(8*1)+(7*1)+(6*6)+(5*1)+(4*5)+(3*9)+(2*2)+(1*4)=111
111 % 10 = 1
So 116159-24-1 is a valid CAS Registry Number.

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116159-24-1Relevant academic research and scientific papers

STUDIES IN POLYETHER SYNTHESIS USING POLYEPOXYDE CYCLISATIONS.

Paterson, Ian,Boddy, Ian,Mason, Ian

, p. 5205 - 5208 (2007/10/02)

The acid-catalysed directed cyclisation of mono-, di-, and triepoxy t-butyl ester derivatives is used for the asymmetric synthesis of various polyether-type fragments including a C13-C27 fragment of etheromycin.The epoxide stereochemistry is set up by Sharpless epoxidation of allylic and homoallylic alcohols.

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