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7-Methoxycoumarin-4-acetic acid

7-Methoxycoumarin-4-acetic acid (CAS 62935-72-2) is a strategically functionalized coumarin derivative engineered for fluorescent probe developmentbioconjugation chemistry, and pharmaceutical scaffold design. This molecule integrates a 7-methoxycoumarin core—a privileged fluorophore scaffold known for blue fluorescence and high quantum yield—with an acetic acid side chain at the C4 position, creating a versatile handle for amide couplingesterification, or bioconjugation to biomolecules. The 7-methoxy substituent enhances electron-donating capacity and fluorescence intensity through intramolecular charge transfer (ICT), while the C4-acetic acid moiety provides orthogonal reactivity for linker attachment without perturbing the coumarin chromophore. This intermediate is particularly valuable for constructing fluorescent labels for protein/DNA taggingFRET pair donors, and CNS-penetrant drug scaffolds where the coumarin-acetate motif balances photophysical properties with synthetic flexibility. Manufactured under controlled conditions, it supports research programs requiring modular access to positionally defined coumarin architectures with tunable emission profiles.

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Product Name
7-Methoxycoumarin-4-acetic acid
CAS Number
62935-72-2
Chinese Name
7-甲氧基香豆素 -4-乙酸
Synonyms
2-(7-Methoxy-2-oxo-2H-chromen-4-yl)acetic acid; 4-Coumarinacetic acid, 7-methoxy-; C₁₂H₁₀O₅ heterocycle; 
Chinese Synonyms
7-甲氧基 -2-氧代 -2H-色烯 -4-乙酸; 7-甲氧基香豆素 -4-乙酸; 甲氧基香豆素乙酸; 荧光香豆素羧酸
Molecular Formula
C₁₂H₁₀O₅
Molecular Weight
234.20 g/mol
Purity
≥ 98% (HPLC area normalization)
Product Category
Fine Chemicals / Fluorescent Dyes / Coumarin Derivatives
Appearance
Off-white to Pale Yellow Crystalline Powder
Melting Point
~210-215°C (estimated, literature reference recommended)
Excitation/Emission
λex ~320-350 nm, λem ~390-420 nm (solvent-dependent, estimated)
Storage Conditions
Store at 2-8°C in amber glass under inert atmosphere. Protect from light, moisture, and strong bases.
Shelf Life
24 months under recommended storage conditions
Packaging
100mg/vial, 500mg/vial, 1g/bottle, 5g/bottle, or customized according to customer requirements
Applications
Fluorescent probe synthesis, protein/DNA labeling via amide coupling, FRET pair donor design, pharmaceutical scaffold development, CNS drug precursor research, optoelectronic material intermediate
Reactivity
Suitable for amide coupling (activation via EDC/HATU), esterification, salt formation, electrophilic aromatic substitution at C6/C8, and coumarin ring functionalization
Special Note
Bioconjugation-Ready Fluorophore—C4-acetic acid enables direct coupling to amines without modifying the 7-methoxy fluorescence core. Distinct from 3-substituted coumarins by emission profile and reactivity. Part of our fluorescent building block series.