Cas 118356-56-2,(2R,5R,6R)-2-tert-Butyl-6-methyl-5-((R)-phenyl-trimethylsilanyl-methyl)-[1,3]dioxan-4-one

118356-56-2

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Basic information

Product Name: (2R,5R,6R)-2-tert-Butyl-6-methyl-5-((R)-phenyl-trimethylsilanyl-methyl)-[1,3]dioxan-4-one
Synonyms: (2R,5R,6R)-2-tert-Butyl-6-methyl-5-((R)-phenyl-trimethylsilanyl-methyl)-[1,3]dioxan-4-one
CAS NO:118356-56-2
Molecular Formula:
Molecular Weight: 334.531
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,5R,6R)-2-tert-Butyl-6-methyl-5-((R)-phenyl-trimethylsilanyl-methyl)-[1,3]dioxan-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (2R,5R,6R)-2-tert-Butyl-6-methyl-5-((R)-phenyl-trimethylsilanyl-methyl)-[1,3]dioxan-4-one(118356-56-2)
EPA Substance Registry System: (2R,5R,6R)-2-tert-Butyl-6-methyl-5-((R)-phenyl-trimethylsilanyl-methyl)-[1,3]dioxan-4-one(118356-56-2)

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: 118356-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118356-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,5 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 118356-56:
(8*1)+(7*1)+(6*8)+(5*3)+(4*5)+(3*6)+(2*5)+(1*6)=132
132 % 10 = 2
So 118356-56-2 is a valid CAS Registry Number.

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118356-56-2Relevant academic research and scientific papers

Direct Michael-Type Addition of Si-Groups to α,β-unsaturated β-Aryl-Substituted Enones with R3SiCl/Bu2Cu(CN)Li2

Amberg, Willi,Seebach, Dieter

, p. 2439 - 2444 (2007/10/02)

(E)-5-Benzylidene-2-tert-butyl-6-methyl-1,3-dioxan-4-one (1) undergoes conjugative silylation (Me3Si, Et3Si, tBuMe2Si, Me2PhSi, products 2-5) with the reagent specified in the title.The reaction is highly diastereoselective, with formal anti addition of R

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