114288-92-5 Usage
Molecular Structure
A cyclohexene carboxylic acid with a 2-[(trimethylsilyl)oxy]and 2-propenyl ester functional groups
Composition
Contains carbon, hydrogen, oxygen, and silicon atoms
Reactivity
Unique molecular structure and reactivity, often used in organic synthesis for various transformations and reactions
Pharmaceutical Industry
Synthesis of drugs and biologically active compounds
Precursor
In the synthesis of specialized materials
Intermediate
In the production of other organic compounds
Potential Applications
Wide range in chemical and pharmaceutical manufacturing
Cyclohexene Carboxylic Acid
A six-membered ring with a double bond and a carboxylic acid group
2-[(trimethylsilyl)oxy]-
A trimethylsilyl group attached to an oxygen atom
2-Propenyl Ester
A propene group attached to an ester functional group
Ester Formation
The carboxylic acid group of the cyclohexene carboxylic acid reacts with the alcohol group of the 2-propenyl alcohol to form an ester linkage
Silylated Compound
The presence of the trimethylsilyl group indicates that the compound is a silylated derivative, which can be used for protection of hydroxyl groups in organic synthesis
Solubility
Likely soluble in organic solvents such as dichloromethane, tetrahydrofuran, or acetone due to its nonpolar nature and the presence of the trimethylsilyl group
Check Digit Verification of cas no
The CAS Registry Mumber 114288-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,8 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 114288-92:
(8*1)+(7*1)+(6*4)+(5*2)+(4*8)+(3*8)+(2*9)+(1*2)=125
125 % 10 = 5
So 114288-92-5 is a valid CAS Registry Number.
114288-92-5Relevant academic research and scientific papers
PREPARATION OF THERMODINAMICALLY STABLE ENOL SILYL ETHERS OF γ,δ-UNSATURATED KETONES BY PALLADIUM-CATALYZED DECARBOXYLATION-ALLYLATION OF ALLYL 2,3-DISUBSTITUTED 3-TRIMETHYLSILOXYACRYLATES
Tsuji, Jiro,Ohashi, Yukihiro,Minami, Ichiro
, p. 2397 - 2398 (2007/10/02)
Allyl 2,3-disubstituted 3-trimethylsiloxyacrylates underwent palladium-catalyzed intramolecular decarboxylation-allylation to afford enol silyl ethers of γ,δ-unsaturated ketones.
