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2H-1-Benzopyran-3-carboxylicacid, 7-(diethylamino)-2-oxo-, 2,5-dioxo-1-pyrrolidinyl ester | 139346-57-9
| Catalog Number | F05-0019 |
| Category | Coumarin |
| Molecular Formula | C18H18 N2 O6 |
| Molecular Weight | 358.35 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| F05-0019 | -- | $-- |
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Product Introduction
7-Diethylamino-3-carboxy-2H-1-benzopyran-2-one is a biological activity pharmaceutical compound. Through its remarkable attributes as a pyrrolidinyl ester, it assumes the pivotal role of efficaciously combating a myriad of ailments, notably encompassing cancer and inflammation.
Chemical Information |
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| Synonyms | N-Succinimidyl 7-(Diethylamino)coumarin-3-carboxylate;N-SUCCINIMIDYL 7-(DIETHYLAMINO)COUMARIN-3-CARBOXYLATE; SUCCINIMIDYL 7-DIETHYLAMINOCOUMARIN-3-CARBOXYLATE; DEAC, SE; 7-(DIETHYLAMINO)COUMARIN-3-CARBOXYLIC ACID N-SUCCINIMIDYL ESTER; 7-DIETHYLAMINOCOUMARIN-3-CARBOXYLIC ACID, SUCCINIMIDYL ESTER |
| Purity | >98.0%(HPLC) |
| IUPAC Name | (2,5-dioxopyrrolidin-1-yl) 7-(diethylamino)-2-oxochromene-3-carboxylate |
| Canonical SMILES | CCN(CC)C1=CC2=C(C=C1)C=C(C(=O)O2)C(=O)ON3C(=O)CCC3=O |
| InChI | InChI=1S/C18H18N2O6/c1-3-19(4-2)12-6-5-11-9-13(17(23)25-14(11)10-12)18(24)26-20-15(21)7-8-16(20)22/h5-6,9-10H,3-4,7-8H2,1-2H3 |
| InChI Key | NUNPVRICKDZFLK-UHFFFAOYSA-N |
| Density | 1.4g/cm3 |
| Appearance | Solid |
| Melting Point | 231 °C |
| MDL Number | MFCD00467585 |
- Product Specification
- Application
| Maximum Absorption Wavelength | 444(H2O) nm |
| Condition To Avoid | Light Sensitive,Moisture Sensitive,Heat Sensitive |
| Storage | 0-10 °C |
| Store Under Inert Gas | Store under inert gas |
2H-1-Benzopyran-3-carboxylic acid 7-(diethylamino)-2-oxo-2,5-dioxo-1-pyrrolidinyl ester is a versatile chemical compound with diverse applications across scientific research and industry. Here are four key applications of this compound:
Fluorescent Dye: Acting as a vibrant fluorescent dye, this compound finds utility in a myriad of biomedical and molecular biology contexts. Its role in labeling and tracking biological molecules such as nucleic acids and proteins within live cells is invaluable. The robust fluorescence signal it emits enables high-resolution imaging in fluorescence microscopy and facilitates precise analysis in flow cytometry, aiding researchers in unraveling the intricacies of biological systems.
Pharmaceutical Research: Within the realm of drug development and screening, this compound serves as a foundational scaffold for crafting novel pharmaceutical agents. Researchers harness its chemical framework to engender potential drugs endowed with specific pharmacological activities. Derivatives derived from this compound may showcase diverse properties ranging from enzyme inhibition to receptor activation and antimicrobial efficacy, representing a promising frontier in the pursuit of innovative therapeutic interventions.
Chemical Sensors: Positioned at the forefront of sensor technology, this compound plays a pivotal role in the design and implementation of chemical sensing devices for detecting an array of analytes in environmental and clinical samples. Its integration into sensor platforms enables the identification of metal ions, pH fluctuations, and small organic molecules with precision and accuracy. These cutting-edge sensors stand as essential tools in environmental monitoring efforts and diagnostic practices.
Material Science: In the realm of material science, this compound serves as a cornerstone in the creation of advanced materials boasting exceptional optical and electronic characteristics. Its integration into polymer matrices and nanomaterials catalyzes the development of functional devices like organic light-emitting diodes (OLEDs) and photovoltaic cells.
Applications of Fluorescent Probes & Dyes
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