Em 450-495 nm Blue
Items 81 to 83 of 83 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
3,4-Dimethylumbelliferone | 2107-78-0 | sc-214171 | 100 mg | $300.00 | ||
3,4-Dimethylumbelliferone is a fluorescent compound that exhibits strong emission in the 450-495 nm range, attributed to its unique coumarin structure. This compound engages in specific π-π stacking interactions, enhancing its photostability and fluorescence intensity. Its ability to undergo intramolecular hydrogen bonding influences its reactivity and solubility in various solvents, while its distinct electronic properties allow for effective energy transfer in biochemical assays. | ||||||
DEAC,SE | 139346-57-9 | sc-495737 | 25 mg | $123.00 | ||
DEAC,SE is a versatile acid halide characterized by its unique reactivity profile, particularly in nucleophilic acyl substitution reactions. Its structure facilitates rapid acylation processes, making it a key player in organic synthesis. The compound exhibits distinct electronic properties that enhance its electrophilicity, promoting efficient interactions with amines and alcohols. Additionally, its ability to form stable intermediates contributes to its utility in various synthetic pathways, showcasing its dynamic behavior in chemical transformations. | ||||||
7-Hydroxycoumarin-3-carboxylic acid, succinimidyl ester | sc-495740 | 50 mg | $119.00 | |||
7-Hydroxycoumarin-3-carboxylic acid, succinimidyl ester, is distinguished by its strong fluorescence emission in the 450-495 nm range, making it an effective probe for studying molecular interactions. Its unique structure allows for selective binding with nucleophiles, facilitating the formation of stable conjugates. The compound's reactivity is influenced by its electron-rich coumarin moiety, which enhances its ability to participate in diverse chemical reactions, showcasing its dynamic role in synthetic chemistry. | ||||||