Cas 193334-92-8,Propanoic acid, 2,2-dimethyl-, [2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-3-oxo-1-cyclohexen-1- yl]methyl ester

193334-92-8

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Basic information

Product Name: Propanoic acid, 2,2-dimethyl-, [2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-3-oxo-1-cyclohexen-1- yl]methyl ester
Synonyms:
CAS NO:193334-92-8
Molecular Formula: C24H36O4Si
Molecular Weight: 416.633
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: Propanoic acid, 2,2-dimethyl-, [2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-3-oxo-1-cyclohexen-1- yl]methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Propanoic acid, 2,2-dimethyl-, [2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-3-oxo-1-cyclohexen-1- yl]methyl ester(193334-92-8)
EPA Substance Registry System: Propanoic acid, 2,2-dimethyl-, [2-[3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]phenyl]-3-oxo-1-cyclohexen-1- yl]methyl ester(193334-92-8)

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: 193334-92-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 193334-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,3,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 193334-92:
(8*1)+(7*9)+(6*3)+(5*3)+(4*3)+(3*4)+(2*9)+(1*2)=148
148 % 10 = 8
So 193334-92-8 is a valid CAS Registry Number.

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193334-92-8Relevant academic research and scientific papers

Cross-coupling approach towards dynemicin analogs without the nitrogen

Bosse, Folkert,Tunoori, Ashok Rao,Maier, Martin E.

, p. 9159 - 9168 (1997)

Utilizing a cross-coupling reaction between the arylstannane 5 and the iodoenone 7, the arylcyclohexenone 8 was prepared. This compound was then transformed into the enediyne aldehydes 16a,b. Treatment of 16a with cat, amounts of TBAF gave rise to the macrocyclic dynemicin analog 17a. This was converted to the phenolic enediyne 18.

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