10543-42-7
10543-42-7
Chemical Structure
Coumarin-6-sulfonyl chloride
Synonym(s): 2-Oxo-2H-chromene-6-sulfonyl chloride
- CAS No.: 10543-42-7
- Formula:C9H5ClO4S
- Molecular Weight:244.65
IUPAC Name: 2-oxo-2H-chromene-6-sulfonyl chloride
InChIKey: HQIPMBGUDSOVEA-UHFFFAOYSA-N
SMILES: O=S(C1=CC=C(O2)C(C=CC2=O)=C1)(Cl)=O
Biological Activity: Coumarin-6-sulfonyl chloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Coumarin-6-sulfonyl chloride | 95.0% | Coumarin-6-sulfonyl chloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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Umbelliferone (Standard) | 99.15% | Umbelliferone (Standard) (7-Hydroxycoumarin (Standard)) is the analytical standard of Umbelliferone (HY-N0573). This product is intended for research and analytical applications. Umbelliferone (7-Hydroxycoumarin), a natural orally active product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent. Umbelliferone induces cell cycle arrest, apoptosis and DNA fragmentation in HepG2 cells. Umbelliferone exhibits significant anticancer effects. Umbelliferone attenuates the alteration characteristics of allergic airway inflammation. Umbelliferone displays the neuroprotective effects and cross the blood-brain barrier. Umbelliferone exhibits anti-inflammatory and antioxidant effects in chronic alcohol-fed rats. | ||||||||||||||||||||
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Herniarin (Standard) | ≥98% | Herniarin (Standard) (Methylumbelliferone (Standard)) is the analytical standard of Herniarin (HY-N1366). This product is intended for research and analytical applications. Herniarin is a natural coumarin occurs in some flowering plants with anticancer effects. Herniarin results in a significant decrease in cell viability by inducing apoptosis in MCF-7 cells. Herniarin also has anti-dermatophytic activity. Herniarin can be used for the study of bladder cancer and breast cancer. | ||||||||||||||||||||
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6-Methylcoumarin | 99.98% | 6-Methylcoumarin is a synthetic fragrance widely used in cosmetics. | ||||||||||||||||||||
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7-Methylcoumarin | 99.61% | 7-Methylcoumarin is a coumarin derivative with potent hepatoprotective and antioxidant properties. 7-Methylcoumarin is a mechanism-based inhibitor for CYP2A6. 7-Methylcoumarin significantly decreases alanine aminotransferase (ALT), aspartate aminotransferase (AST), and serum bilirubin (TB) in rats with CCl4-induced liver damage, whilst restoring total protein (TP) and albumin (TA) levels in serum as well as preventing oxidative stress. 7-Methylcoumarin can decline mitotic activity of A. sativum promeristem. | ||||||||||||||||||||
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6-Hydroxycoumarin (Standard) | ≥98% | 6-Hydroxycoumarin (Standard) is the analytical standard of 6-Hydroxycoumarin (HY-N6656). This product is intended for research and analytical applications. 6-Hydroxycoumarin is a plant-derived secondary metabolite of the coumarin class, possessing insecticidal, antitumor, and other biological activities. 6-Hydroxycoumarin targets the midgut tissue of the red imported fire ant (Solenopsis invicta), inhibits CYP450, induces elevated activities of GST, CarE, and SOD, disrupts mitochondrial ultrastructure, triggers apoptosis, and also impairs insect neuromuscular behavior. 6-Hydroxycoumarin exhibits photoallergic properties and serves as an intermediate for the synthesis of isoxazolyl and triazolyl derivatives. 6-Hydroxycoumarin is applicable to research related to red imported fire ant control. | ||||||||||||||||||||
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6-Bromocoumarin | 6-Bromocoumarin (compound 34) is a potential anti-bacterial agent, with no inhibition against 17β-HSD1. 6-Bromocoumarin exhibtis affinity for α and β estrogen receptors. | |||||||||||||||||||||
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Coumarin boronic acid | 99.93% | Coumarin boronic acid is a fluorescent probe. The excitation and emission wavelengths of coumarin boronic acid are set to 360 nm and 430 nm, respectively. Coumarin boronic acid can be used to monitor the formation of amino acid and protein hydroxyl peroxides in real time, which is beneficial for understanding the mechanisms of oxidative stress and protein post-translational modification. | ||||||||||||||||||||
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6-Aminocoumarin hydrochloride | 6-Aminocoumarin hydrochloride is a coumarin dye, which belongs to the donor-acceptor compounds as it contains a donor amine group and an acceptor carbonyl group. | |||||||||||||||||||||
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7-Aminocoumarin | 7-Aminocoumarin is highly fluorescent, acts as an optical brightener and fluorescent probe. | |||||||||||||||||||||
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Umbelliferone-13C6 | Umbelliferone-13C6 (7-Hydroxycoumarin-13C6) is the 13C-labeled Umbelliferone (HY-N0573). Umbelliferone (7-Hydroxycoumarin), a natural orally active product of the coumarin family, is a fluorescing compound which can be used as a sunscreen agent. Umbelliferone induces cell cycle arrest, apoptosis and DNA fragmentation in HepG2 cells. Umbelliferone exhibits significant anticancer effects. Umbelliferone attenuates the alteration characteristics of allergic airway inflammation. Umbelliferone displays the neuroprotective effects and cross the blood-brain barrier. Umbelliferone exhibits anti-inflammatory and antioxidant effects in chronic alcohol-fed rats. | |||||||||||||||||||||
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