69114-02-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 11 carbon (C) atoms, 12 hydrogen (H) atoms, and 4 oxygen (O) atoms.
Explanation
This describes the specific arrangement of atoms and functional groups in the molecule. The molecule consists of a phenyl group (a six-membered carbon ring with alternating single and double bonds) with a methoxy group (-OCH3) at the 3-position and an oxiran-2-ylmethoxy group (-OCH2CH2O) at the 4-position. The molecule also contains an ethanone group (a two-carbon chain with a carbonyl group, C=O, at one end).
Explanation
These are the specific functional groups present in the molecule, which give it its unique chemical properties. The ketone group (C=O) is present in the ethanone part of the molecule, while the phenyl, methoxy, and oxiran-2-ylmethoxy groups are attached to the phenyl ring.
Explanation
The compound is classified as a derivative of a ketone, which is a type of organic compound containing a carbonyl group (C=O) bonded to two other carbon atoms.
Explanation
1-[3-METHOXY-4-(OXIRAN-2-YLMETHOXY)PHENYL]ETHANONE is used in various fields, including the synthesis of other organic compounds, research in the pharmaceutical industry, and the development of new drugs. It may also serve as a building block for the production of other organic compounds.
Explanation
The solubility of a compound is its ability to dissolve in a solvent, such as water or organic solvents like ethanol or acetone. The solubility of 1-[3-METHOXY-4-(OXIRAN-2-YLMETHOXY)PHENYL]ETHANONE is not provided in the material, but it would depend on the specific solvent used.
Explanation
The stability of a compound refers to its ability to resist decomposition or reaction under certain conditions. The stability of 1-[3-METHOXY-4-(OXIRAN-2-YLMETHOXY)PHENYL]ETHANONE is not provided in the material, but it would depend on factors such as temperature, pressure, and the presence of other reactive substances.
Chemical Structure
1-[3-Methoxy-4-(oxiran-2-ylmethoxy)phenyl]ethanone
Functional Groups
Ketone, Phenyl, Methoxy, Oxiran-2-ylmethoxy
Type of Compound
Ketone derivative
Applications
Organic synthesis, pharmaceutical research, potential drug development, building block for other organic compounds
Solubility
Unknown (depends on the solvent)
Stability
Unknown (depends on environmental conditions)
Check Digit Verification of cas no
The CAS Registry Mumber 69114-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,1 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69114-02:
(7*6)+(6*9)+(5*1)+(4*1)+(3*4)+(2*0)+(1*2)=119
119 % 10 = 9
So 69114-02-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O4/c1-8(13)9-3-4-11(12(5-9)14-2)16-7-10-6-15-10/h3-5,10H,6-7H2,1-2H3
69114-02-9Relevant academic research and scientific papers
Fache,Boutevin,Caillol
, p. 712 - 725 (2016)
Epoxy thermosets were prepared from mixtures of phenolics modelling the product stream of the lignin-to-vanillin process. Vanillin is one of the only mono-aromatic compounds produced on an industrial scale from lignin. This process leads to mixtures of phenolic compounds. Isolation of pure vanillin is costly both economically and environmentally. The present work demonstrates that these purification steps are not necessary in order to prepare high-performance epoxy thermosets from biomass. Model mixtures of depolymerization products of lignins from both softwood and hardwood were prepared. These mixtures were subjected in a first step to a Dakin oxidation in order to increase their phenolic functionality. In the second step, they were glycidylated to obtain mixtures of epoxy monomers. Each of the components of the mixtures was individually subjected to the same reactions to provide further insights on their reactivity. Epoxy thermosets were conveniently prepared from these epoxy monomer mixtures. These potentially bio-based epoxy thermosets displayed outstanding thermo-mechanical properties while avoiding environmentally damaging purification steps. Thus, their production could advantageously be integrated in a biorefinery as a high value added product from lignin processing.
