Atomfair ((o-Methoxyphenoxy)methyl)oxirane C10H12O3

Description ((o-Methoxyphenoxy)methyl)oxirane (CAS No. 2210-74-4) is a high-purity epoxide compound with the molecular formula C10H12O3and IUPAC name 2-[(2-methoxyphenoxy)methyl]oxirane. This specialty chemical features a reactive oxirane (epoxide) ring and a methoxyphenoxy moiety, making it a versatile intermediate for organic synthesis and pharmaceutical applications. It is supplied as a clear to pale-yellow liquid with a characteristic aromatic odor and is recommended for use under controlled conditions due to its reactivity. Ideal for researchers in medicinal chemistry and material science, this compound is rigorously tested for purity and stability, ensuring reliable performance in advanced synthetic workflows. Store in a cool, dry place under…

Description

((o-Methoxyphenoxy)methyl)oxirane (CAS No. 2210-74-4) is a high-purity epoxide compound with the molecular formula C₁₀H₁₂O₃ and IUPAC name 2-[(2-methoxyphenoxy)methyl]oxirane. This specialty chemical features a reactive oxirane (epoxide) ring and a methoxyphenoxy moiety, making it a versatile intermediate for organic synthesis and pharmaceutical applications. It is supplied as a clear to pale-yellow liquid with a characteristic aromatic odor and is recommended for use under controlled conditions due to its reactivity. Ideal for researchers in medicinal chemistry and material science, this compound is rigorously tested for purity and stability, ensuring reliable performance in advanced synthetic workflows. Store in a cool, dry place under inert atmosphere to maintain integrity.

CAS No: 2210-74-4
Molecular Formula: C10H12O3
Molecular Weight: 180.20
Exact Mass: 180.078644241
Monoisotopic Mass: 180.078644241
IUPAC Name: 2-[(2-methoxyphenoxy)methyl]oxirane
SMILES: COC1=CC=CC=C1OCC2CO2
Synonyms: ((o-Methoxyphenoxy)methyl)oxirane, [(o-methoxyphenoxy)methyl]oxirane, 218-644-8, 2210-74-4, 1-(2-Methoxyphenoxy)-2,3-epoxypropane

Application

((o-Methoxyphenoxy)methyl)oxirane is primarily used as a key intermediate in the synthesis of bioactive molecules, including potential pharmaceuticals and agrochemicals. Its epoxide group enables ring-opening reactions for creating polyether or polyol derivatives. Researchers also employ it in polymer modification and crosslinking applications due to its bifunctional reactivity. Suitable for developing epoxy resins with tailored properties for coatings or adhesives.

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