4-Hydroxycoumarin CAS#1076-38-6

  • Highly Versatile Intermediate: Based on a coumarin scaffold, it is widely used in the synthesis of diverse organic compounds.

  • Dual Reactivity: Possesses both electrophilic and nucleophilic properties, enabling flexible participation in various chemical reactions.

  • Defined Physical Characteristics: Exhibits a clear melting point (206°C) and needle-shaped crystalline form, supporting consistent handling and processing.

  • Good Solubility Profile: Easily soluble in ethanol, ether, and hot water, facilitating use in multiple solvent systems and applications.


 

Product Description: 4-Hydroxycoumarin (CAS# 1076-38-6)

4-Hydroxycoumarin is a derivative of coumarin and represents a highly versatile heterocyclic scaffold widely used in the synthesis of a variety of organic compounds. It exhibits both electrophilic and nucleophilic reactivity. The product appears as slightly yellow, needle-like crystals with a melting point of 206°C. It is readily soluble in ethanol, ether, and hot water, and produces a brown coloration when reacting with ferric chloride.1777340371859027.jpg.webp

4-Hydroxycoumarin Chemical Properties

Melting point 211-213 °C (lit.)
Boiling point 228.82°C (rough estimate)
Density 1.1734 (rough estimate)
Vapor pressure 0.02Pa at 25℃
Refractive index 1.4500 (estimate)
Storage tempStore below +30°C.
Solubility DMSO (Slightly), Methanol (Slightly)
Form Liquid
Pka4.50±1.00(Predicted)
Color Clear colorless to slightly yellow
Water Solubility PRACTICALLY INSOLUBLE
BRN 129768
InChIKeyVXIXUWQIVKSKSA-UHFFFAOYSA-N
LogP1.6-2.31 at 21.2℃
CAS DataBase Reference1076-38-6(CAS DataBase Reference)
NIST Chemistry Reference4-Hydroxycoumarin(1076-38-6)
EPA Substance Registry System2H-1-Benzopyran-2-one, 4-hydroxy- (1076-38-6)
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS DJ3100000
Hazard Note Irritant
TSCA Yes
HS Code 29322980

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Product Application: 4-Hydroxycoumarin (CAS# 1076-38-6)

4-Hydroxycoumarin is widely used as an intermediate in the production of pharmaceuticals and pesticides. It serves as a key precursor for anticoagulant compounds such as dicoumarol, new anticoagulants, and warfarin, which belong to a class of oral anticoagulants. Among these, dicoumarol has a relatively long duration of action (4–7 days), while coumarin ethyl ester exhibits a shorter duration (2–3 days).

In addition, 4-hydroxycoumarin is utilized in the synthesis of certain rodenticides. It also has applications in the flavor and fragrance industry, as coumarin compounds are widely found in plants.1777340390102154.jpg.webp

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