Cas 120019-59-2,1-[(1S,2S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenyl-cyclohex-3-enyl]-ethanone

120019-59-2

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Basic information

Product Name: 1-[(1S,2S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenyl-cyclohex-3-enyl]-ethanone
Synonyms:
CAS NO:120019-59-2
Molecular Formula:
Molecular Weight: 430.66
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: 1-[(1S,2S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenyl-cyclohex-3-enyl]-ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(1S,2S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenyl-cyclohex-3-enyl]-ethanone(120019-59-2)
EPA Substance Registry System: 1-[(1S,2S,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-phenyl-cyclohex-3-enyl]-ethanone(120019-59-2)

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: 120019-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120019-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,0,1 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 120019-59:
(8*1)+(7*2)+(6*0)+(5*0)+(4*1)+(3*9)+(2*5)+(1*9)=72
72 % 10 = 2
So 120019-59-2 is a valid CAS Registry Number.

120019-59-2Upstream product

120019-59-2Downstream Products

120019-60-5 (3S,4S,5S)-4-Acetyl-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-5-phenyl-cyclohexanone

120019-59-2Relevant academic research and scientific papers

Possible Mechanism for the Stereoselective Double Michael Reaction Catalyzed by Trityl Perchlorate

Kobayashi, Shu,Sagawa, Yukihiro,Akamatsu, Hiroshi,Mukaiyama, Teruaki

, p. 1777 - 1780 (1988)

The trityl perchlorate catalyzed double Michael reaction forming six-membered ring compounds from α,β-unsaturated ketones and siloxydienes was shown to take place via a two step process.

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