Atomfair Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate C11H12O4 CAS 114077-42-8

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.

Properties

• CAS Number: 114077-42-8
• Complexity: 247
• IUPAC Name: methyl (E)-2-(2-hydroxyphenyl)-3-methoxy-prop-2-enoate
• InChI: InChI=1S/C11H12O4/c1-14-7-9(11(13)15-2)8-5-3-4-6-10(8)12/h3-7,12H,1-2H3/b9-7+
• InChI Key: CUEDLSLTSIRGCF-VQHVLOKHSA-N
• Exact Mass: 208.07355886
• Molecular Formula: C11H12O4
• Molecular Weight: 208.21
• SMILES: CO/C=C(C1=CC=CC=C1O)/C(=O)OC
• Topological: 55.8
• Monoisotopic Mass: 208.07355886
• Synonyms: 125808-20-0, DTXSID60558991, Methyl (2E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate, DTXCID10509771, (e)-methyl 2-(2-hydroxyphenyl)-3-methoxyacrylate, 114077-42-8, Methyl 2-(2-hydroxyphenyl)-3-methoxyacrylate, methyl (E)-2-(2-hydroxyphenyl)-3-methoxyprop-2-enoate, Methyl 2-(2′-hydroxy phenyl)-3-methoxy acrylate, METHYL 2-(2-HYDROXYPHENYL)-3-METHOXYPROP-2-ENOATE, SCHEMBL710656, CUEDLSLTSIRGCF-VQHVLOKHSA-N, AKOS015895802, CS-0263848, H40469, (e)-methyl2-(2-hydroxyphenyl)-3-methoxyacrylate, (Z)-methyl 2-(2-hydroxyphenyl)-3-methoxyacrylate, (E)-methyl 2-(2′-hydroxyphenyl)-3-methoxyacrylate, (E)-methyl 2-(2-hydroxyphenyl)-3-methoxypropenoate, E-methyl 3-methoxy-2-(2′-hydroxyphenyl)propenoate, Benzeneacetic acid, 2-hydroxy-alpha-(methoxymethylene)-, methyl ester, Benzeneacetic acid, 2-hydroxy-|A-(methoxymethylene)-, methyl ester, (|AE)-

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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