6-HYDROXY-4,4,5,7,8-PENTAMETHYL-3,4-DIHYDROCOUMARIN

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Reagent Code: #196352
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CAS Number 40662-76-8

science Other reagents with same CAS 40662-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.29 g/mol
Formula C₁₄H₁₈O₃
badge Registry Numbers
MDL Number MFCD26394817
thermostat Physical Properties
Melting Point 117 °C
Boiling Point 366.9±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.118±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of anticoagulant compounds and fluorescent dyes. It also serves as a building block in the development of certain pharmaceuticals due to its structural similarity to coumarin derivatives known for biological activity. Its hydroxyl and methyl-substituted ring system makes it suitable for use in antioxidant research and as a precursor in the synthesis of more complex heterocyclic systems. Additionally, it finds application in the study of photochemical properties owing to its conjugated structure.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,480.00
inventory 250mg
10-20 days ฿2,470.00
inventory 1g
10-20 days ฿4,940.00

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6-HYDROXY-4,4,5,7,8-PENTAMETHYL-3,4-DIHYDROCOUMARIN
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Used as an intermediate in organic synthesis, particularly in the preparation of anticoagulant compounds and fluorescent dyes. It also serves as a building block in the development of certain pharmaceuticals due to its structural similarity to coumarin derivatives known for biological activity. Its hydroxyl and methyl-substituted ring system makes it suitable for use in antioxidant research and as a precursor in the synthesis of more complex heterocyclic systems. Additionally, it finds application in the

Used as an intermediate in organic synthesis, particularly in the preparation of anticoagulant compounds and fluorescent dyes. It also serves as a building block in the development of certain pharmaceuticals due to its structural similarity to coumarin derivatives known for biological activity. Its hydroxyl and methyl-substituted ring system makes it suitable for use in antioxidant research and as a precursor in the synthesis of more complex heterocyclic systems. Additionally, it finds application in the study of photochemical properties owing to its conjugated structure.

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