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| | 3-Cyano-7-hydroxycoumarin Basic information |
| Product Name: | 3-Cyano-7-hydroxycoumarin | | Synonyms: | 3-CYANO-7-HYDROXYCOUMARIN;3-CYANOUMBELLIFERONE, FOR FLUORESCENCE*;7-hydroxy-2-oxo-2H-chromene-3-carbonitrile;7-Hydroxy-2-oxochromene-3-carbonitrile;3-CyanouMbelliferone [3-Cyano-7-hydroxycouMarin];3-Cyano-7-hydroxycoumarin *CAS 19088-73-4*;7-hydroxy-2-oxo-1-benzopyran-3-carbonitrile;3-Cyano-7-hydroxycoumarin 95+% | | CAS: | 19088-73-4 | | MF: | C10H5NO3 | | MW: | 187.15 | | EINECS: | 200-123-4 | | Product Categories: | heterocyclic/Aliphatic series;AMCA | | Mol File: | 19088-73-4.mol |  |
| | 3-Cyano-7-hydroxycoumarin Chemical Properties |
| Melting point | ≥250 °C(lit.) | | Boiling point | 436.6±45.0 °C(Predicted) | | density | 1.50±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | DMF: soluble | | pka | 7.03 ± 0.20, most acidic, temperature:
25 °C | | form | powder to crystal | | color | Yellow solid or powder | | λmax | 408 nm (Buffer pH 9); 408 nm
(MeOH) | | BRN | 153271 | | Major Application | Electroluminescentdevice;laser dyes; modified polyester for foodcontainers/beverage bottles; monitoring of cationicphotopolymerization processes;textiles;thin films | | Biological Applications | Detectingmicroorganisms,nucleic acids; inhibiting cellproliferation/tumor growth; reference standard foresters; ethers,phosphates substrates; asa substrate for measuring nucleic acid polymerasesactivity; treating viral or parasite infections | | InChI | 1S/C10H5NO3/c11-5-7-3-6-1-2-8(12)4-9(6)14-10(7)13/h1-4,12H | | InChIKey | IJQYTHQDUDCJEQ-UHFFFAOYSA-N | | SMILES | Oc1ccc2C=C(C#N)C(=O)Oc2c1 | | CAS DataBase Reference | 19088-73-4 |
| Hazard Codes | Xn | | Risk Statements | 20/21/22-36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | F | 8 | | HS Code | 2932.20.4500 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| | 3-Cyano-7-hydroxycoumarin Usage And Synthesis |
| Uses | 3-Cyano-7-hydroxycoumarin has been the most widely used fluorophores for preparing fluorogenic substrates.As a blue-fluorescent probe used as a reference standard. | | Uses | 3-Cyanoumbelliferone is a calibration standard. | | Synthesis | GENERAL METHOD: α-substituted ethyl acetate (1.0 mmol) and phenyl iododo diacetate (1.0 mmol) were dissolved in ethanol (5 mL) under continuous stirring conditions. After 10 min of reaction, benzaldehyde or salicylaldehyde (1.0 mmol) was added to the system and the reaction was continued with stirring until the appropriate time. The progress of the reaction was monitored by thin layer chromatography (TLC). After the TLC showed that the reaction was complete, the ethanol was evaporated under reduced pressure. Subsequently, the product was extracted with ethyl acetate and the organic phase was dried with anhydrous sodium sulfate (Na2SO4) and concentrated again under reduced pressure to remove the solvent. The resulting crude product was purified by recrystallization from a solvent mixture of ethyl acetate and hexane to finally obtain the target compound 7-hydroxy-2-oxochromene-3-carbonitrile (3a-3h and 4a-4r series derivatives). | | References | [1] Synthetic Communications, 2005, vol. 35, # 6, p. 785 - 790
[2] Phosphorus, Sulfur and Silicon and the Related Elements, 2002, vol. 177, # 11, p. 2555 - 2559
[3] Tetrahedron Letters, 2017, vol. 58, # 32, p. 3183 - 3187
[4] Journal of Heterocyclic Chemistry, 2007, vol. 44, # 4, p. 867 - 870
[5] Journal of the Iranian Chemical Society, 2016, vol. 13, # 1, p. 149 - 153 |
| | 3-Cyano-7-hydroxycoumarin Preparation Products And Raw materials |
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