2-(4-((2,4-Dioxothiazolidin-5-yl)methyl)phenoxy)acetic acid

98%

Reagent Code: #171326
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CAS Number 179087-93-5

science Other reagents with same CAS 179087-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.28 g/mol
Formula C₁₂H₁₁NO₅S
badge Registry Numbers
MDL Number MFCD11113230
thermostat Physical Properties
Boiling Point 540.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antidiabetic agents. It serves as a key building block in the preparation of thiazolidinedione derivatives, which act as insulin sensitizers in the treatment of type 2 diabetes. The compound's structure allows for effective binding to peroxisome proliferator-activated receptors (PPARs), enhancing glucose uptake and improving insulin resistance. It is also employed in research settings to explore new bioactive molecules with metabolic regulatory effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,200.00
inventory 100mg
10-20 days ฿6,060.00
inventory 250mg
10-20 days ฿10,210.00

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2-(4-((2,4-Dioxothiazolidin-5-yl)methyl)phenoxy)acetic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of antidiabetic agents. It serves as a key building block in the preparation of thiazolidinedione derivatives, which act as insulin sensitizers in the treatment of type 2 diabetes. The compound's structure allows for effective binding to peroxisome proliferator-activated receptors (PPARs), enhancing glucose uptake and improving insulin resistance. It is also employed in research settings to explore new bioactive molecu

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antidiabetic agents. It serves as a key building block in the preparation of thiazolidinedione derivatives, which act as insulin sensitizers in the treatment of type 2 diabetes. The compound's structure allows for effective binding to peroxisome proliferator-activated receptors (PPARs), enhancing glucose uptake and improving insulin resistance. It is also employed in research settings to explore new bioactive molecules with metabolic regulatory effects.

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