2-Carbethoxy-3-(2-thienyl)propionic acid

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Reagent Code: #44729
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CAS Number 143468-96-6

science Other reagents with same CAS 143468-96-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.2649 g/mol
Formula C₁₀H₁₂O₄S
thermostat Physical Properties
Boiling Point 361.9 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.295g/cm3
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting cardiovascular and neurological disorders. Its structure, featuring a thienyl group, makes it a valuable intermediate in the production of compounds with potential anti-inflammatory and analgesic properties. Additionally, it serves as a key building block in organic synthesis, enabling the creation of complex molecules for research and industrial applications. Its ester functional group allows for further chemical modifications, making it versatile in medicinal chemistry and drug discovery processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,040.00

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2-Carbethoxy-3-(2-thienyl)propionic acid
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This compound is primarily utilized in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting cardiovascular and neurological disorders. Its structure, featuring a thienyl group, makes it a valuable intermediate in the production of compounds with potential anti-inflammatory and analgesic properties. Additionally, it serves as a key building block in organic synthesis, enabling the creation of complex molecules for research and industrial applications. Its este

This compound is primarily utilized in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting cardiovascular and neurological disorders. Its structure, featuring a thienyl group, makes it a valuable intermediate in the production of compounds with potential anti-inflammatory and analgesic properties. Additionally, it serves as a key building block in organic synthesis, enabling the creation of complex molecules for research and industrial applications. Its ester functional group allows for further chemical modifications, making it versatile in medicinal chemistry and drug discovery processes.

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