4-Methyl-1,2-dithiolane-4-carboxylic acid

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Reagent Code: #130870
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CAS Number 208243-72-5

science Other reagents with same CAS 208243-72-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.25 g/mol
Formula C₅H₈O₂S₂
badge Registry Numbers
MDL Number MFCD11042354
thermostat Physical Properties
Boiling Point 305.7±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.387±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in developing drugs with antioxidant and anti-inflammatory properties. It plays a role in the preparation of biologically active molecules that mimic the effects of lipoic acid, supporting cellular energy production and protecting against oxidative stress. Also utilized in research settings to design novel compounds for metabolic and neurodegenerative disease studies. Its dithiolane ring structure enables redox activity, making it valuable in medicinal chemistry for creating compounds that can regenerate endogenous antioxidants like glutathione.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,680.00
inventory 250mg
10-20 days ฿7,000.00

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4-Methyl-1,2-dithiolane-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in developing drugs with antioxidant and anti-inflammatory properties. It plays a role in the preparation of biologically active molecules that mimic the effects of lipoic acid, supporting cellular energy production and protecting against oxidative stress. Also utilized in research settings to design novel compounds for metabolic and neurodegenerative disease studies. Its dithiolane ring structure enables redox activity, making

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in developing drugs with antioxidant and anti-inflammatory properties. It plays a role in the preparation of biologically active molecules that mimic the effects of lipoic acid, supporting cellular energy production and protecting against oxidative stress. Also utilized in research settings to design novel compounds for metabolic and neurodegenerative disease studies. Its dithiolane ring structure enables redox activity, making it valuable in medicinal chemistry for creating compounds that can regenerate endogenous antioxidants like glutathione.

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