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Atomfair Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate C11H12O4
Description Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate (CAS No. 114077-42-8) is a high-purity organic compound with the molecular formula C11H12O4. This ester derivative features a conjugated system with an (E)-configured double bond, a 2-hydroxyphenyl group, and a methoxyacrylate moiety, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. Its precise structure, confirmed by NMR and HPLC analysis, ensures reliability for advanced applications. Ideal for researchers exploring bioactive molecules, this compound is supplied in rigorously controlled conditions to guarantee stability and performance. Available in various quantities to meet both lab-scale and bulk requirements.
Description
Description
Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate (CAS No. 114077-42-8) is a high-purity organic compound with the molecular formula C11H12O4. This ester derivative features a conjugated system with an (E)-configured double bond, a 2-hydroxyphenyl group, and a methoxyacrylate moiety, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. Its precise structure, confirmed by NMR and HPLC analysis, ensures reliability for advanced applications. Ideal for researchers exploring bioactive molecules, this compound is supplied in rigorously controlled conditions to guarantee stability and performance. Available in various quantities to meet both lab-scale and bulk requirements.
- CAS No: 114077-42-8
- Molecular Formula: C11H12O4
- Molecular Weight: 208.21
- Exact Mass: 208.07355886
- Monoisotopic Mass: 208.07355886
- IUPAC Name: methyl (E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate
- SMILES: CO/C=C(C1=CC=CC=C1O)/C(=O)OC
- Synonyms: 125808-20-0, DTXSID60558991, Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate, DTXCID10509771, (e)-methyl 2-(2-hydroxyphenyl)-3-methoxyacrylate
Application
Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate is primarily used as a key synthetic intermediate in the development of pharmaceuticals and agrochemicals. Its reactive enoate and phenolic groups make it suitable for constructing complex heterocycles or as a precursor for bioactive molecules. Researchers also employ it in studies involving anti-inflammatory or antioxidant compounds due to its structural resemblance to natural phenolic derivatives. Additionally, it serves as a model substrate in organic synthesis methodologies, such as cross-coupling or cyclization reactions.
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