Ethyl 5-hydroxy-3,6-dihydro-2H-pyran-4-carboxylate

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Reagent Code: #180741
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CAS Number 324767-92-2

science Other reagents with same CAS 324767-92-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₈H₁₂O₄
badge Registry Numbers
MDL Number MFCD17676281
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antidiabetic agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in ring-opening, ester hydrolysis, and reduction reactions to generate bioactive molecules. Also utilized in the preparation of prodrugs due to the presence of both ester and hydroxyl groups, which can be tailored for improved metabolic stability and absorption.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,630.00
inventory 250mg
10-20 days ฿6,660.00
inventory 1g
10-20 days ฿18,150.00

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Ethyl 5-hydroxy-3,6-dihydro-2H-pyran-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antidiabetic agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in ring-opening, ester hydrolysis, and reduction reactions to generate bioactive molecules. Also utilized in the preparation of prodrugs due to the presence of both ester and hydroxyl groups, which can be tailored for impro

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antidiabetic agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in ring-opening, ester hydrolysis, and reduction reactions to generate bioactive molecules. Also utilized in the preparation of prodrugs due to the presence of both ester and hydroxyl groups, which can be tailored for improved metabolic stability and absorption.

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