CAS 1076-38-6
:4-Hydroxycoumarin
Description:
4-Hydroxycoumarin is an organic compound belonging to the coumarin family, characterized by its aromatic structure featuring a benzopyrone moiety. It appears as a white to pale yellow crystalline solid and is known for its distinct sweet, herbaceous odor. This compound is soluble in organic solvents such as ethanol and ether but has limited solubility in water. 4-Hydroxycoumarin exhibits various biological activities, including anticoagulant properties, making it relevant in medicinal chemistry, particularly as a precursor for the synthesis of anticoagulant drugs like warfarin. Additionally, it has applications in the fields of fluorescence and photochemistry due to its ability to absorb ultraviolet light and emit fluorescence. The compound can undergo various chemical reactions, including oxidation and esterification, which can modify its properties and enhance its utility in different applications. Safety considerations include potential skin irritation and toxicity, necessitating appropriate handling measures in laboratory settings. Overall, 4-Hydroxycoumarin is a versatile compound with significant implications in both research and pharmaceutical development.
Formula:C9H6O3
InChI:InChI=1S/C9H6O3/c10-7-5-9(11)12-8-4-2-1-3-6(7)8/h1-5,10H
InChI key:InChIKey=VXIXUWQIVKSKSA-UHFFFAOYSA-N
SMILES:OC=1C=2C(OC(=O)C1)=CC=CC2
Synonyms:- 2-hydroxy-4H-chromen-4-one
- 2H-1-Benzopyran-2-one, 4-hydroxy-
- 4-Coumarinol
- 4-Coumarinyl Alcohol
- 4-Hidroxicumarina
- 4-Hydroxy Coumarin
- 4-Hydroxy-1-Benzopyran-2-One
- 4-Hydroxy-2H-1-benzopyran-2-one
- 4-Hydroxy-2H-benzo[b]pyran-2-one
- 4-Hydroxy-2H-benzopyran-2-one
- 4-Hydroxy-chromen-2-one
- 4-Hydroxychromen-2-one
- 4-Hydroxycoumariin
- 4-Hydroxycoumarine
- 4-Hydroxycumarin
- 4-[(1E)-3-hydroxyprop-1-en-1-yl]phenol
- 4-hydroxy-2H-chromen-2-one
- Benzotetronic acid
- Coumarin, 4-Hydroxy-
- Naian
- Nsc 11889
- See more synonyms
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Found 17 products.
4-Hydroxycoumarin
CAS:Formula:C9H6O3Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow powder to crystalMolecular weight:162.144-Hydroxycoumarin, 98+%
CAS:<p>4-Hydroxycoumarin is involved in annulation reactions, due to the relatively high acidity of the C-H bond at the 3-position: a three-component reaction with isocyanides and dialkyl acetylene dicarboxylates affords annulated 4H-pyrans. This Thermo Scientific Chemicals brand product was originally par</p>Formula:C9H6O3Purity:98+%Color and Shape:Crystals or powder or crystalline powder, White to pale creamMolecular weight:162.144-Hydroxycoumarin
CAS:4-Hydroxycoumarin analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C9H6O3Purity:(HPLC) ≥95%Color and Shape:PowderMolecular weight:162.154-Hydroxycoumarin
CAS:<p>4-Hydroxycoumarin: precursor to 4HC anticoagulants like warfarin; has anticoagulant, antibacterial, antiviral, and anticancer properties.</p>Formula:C9H6O3Purity:≥98%Color and Shape:Light Yellow To Brown Crystalline PowderMolecular weight:162.144-Hydroxycoumarin
CAS:Formula:C9H6O3Purity:≥ 98.0%Color and Shape:White to off-white crystalline powderMolecular weight:162.14Warfarin EP Impurity B (4-Hydroxy Coumarin)
CAS:Formula:C9H6O3Color and Shape:White To Off-White SolidMolecular weight:162.14Warfarin EP Impurity B
CAS:Controlled ProductFormula:C9H6O3Color and Shape:NeatMolecular weight:162.144-Hydroxycoumarin
CAS:<p>4-Hydroxycoumarin</p>Formula:C9H6O3Purity:98%Color and Shape: off white powderMolecular weight:162.14214g/mol4-Hydroxy Coumarin
CAS:Controlled Product<p>Applications 4-Hydroxy Coumarin is a plant derived antioxidant, protecting against lipid peroxidation, as well as a potential inhibitor of HIV-1 Integrase.<br>References Foti, M. et al.: J. Agric. F., 44, 497 (1996); J. Med. Chem., 40, 242 (1997);<br></p>Formula:C9H6O3Color and Shape:NeatMolecular weight:162.144-Hydroxycoumarin
CAS:<p>4-Hydroxycoumarin is a synthetic organic compound, which is a derivative of coumarin. This compound derives from a benzopyrone structure, specifically known as a precursor in the synthesis of various anticoagulant agents. Its mode of action involves the inhibition of the enzyme vitamin K epoxide reductase. This inhibition subsequently decreases the synthesis of active clotting factors II, VII, IX, and X by preventing the regeneration of reduced vitamin K.</p>Formula:C9H6O3Purity:Min. 97.5 Area-%Color and Shape:PowderMolecular weight:162.14 g/mol















