Cas 105590-61-2,(3S,4S)-3-[(S)-(tert-Butyl-dimethyl-silanyloxy)-phenyl-methyl]-4,8-diphenyl-octane-2,6-dione

105590-61-2

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Basic information

Product Name: (3S,4S)-3-[(S)-(tert-Butyl-dimethyl-silanyloxy)-phenyl-methyl]-4,8-diphenyl-octane-2,6-dione
Synonyms:
CAS NO:105590-61-2
Molecular Formula:
Molecular Weight: 514.78
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: (3S,4S)-3-[(S)-(tert-Butyl-dimethyl-silanyloxy)-phenyl-methyl]-4,8-diphenyl-octane-2,6-dione(CAS DataBase Reference)
NIST Chemistry Reference: (3S,4S)-3-[(S)-(tert-Butyl-dimethyl-silanyloxy)-phenyl-methyl]-4,8-diphenyl-octane-2,6-dione(105590-61-2)
EPA Substance Registry System: (3S,4S)-3-[(S)-(tert-Butyl-dimethyl-silanyloxy)-phenyl-methyl]-4,8-diphenyl-octane-2,6-dione(105590-61-2)

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: 105590-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 105590-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,5,9 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 105590-61:
(8*1)+(7*0)+(6*5)+(5*5)+(4*9)+(3*0)+(2*6)+(1*1)=112
112 % 10 = 2
So 105590-61-2 is a valid CAS Registry Number.

105590-61-2Upstream product

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105590-61-2Relevant academic research and scientific papers

TRITYL PERCHLORATE CATALYZED TANDEM MICHAEL-ALDOL REACTION. A FACILE METHOD FOR THE STEREOSELECTIVE SYNTHESES OF γ-ACYL SUBSTITUTED δ-HYDROXY KETONE DERIVATIVES

Kobayashi, Shu,Mukaiyama, Teruaki

, p. 221 - 224 (2007/10/02)

In the presence of a catalytic amount of trityl perchlorate, the intermediate adducts, produced in situ by the conjugate addition of silyl enol ethers with α,β-unsaturated ketones, react with aldehydes to give the corresponding γ-acyl substituted δ-hydrox

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