Methyl 2,5-Dihydrothiophene-3-carboxylate

95%

Reagent Code: #208129
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CAS Number 67488-46-4

science Other reagents with same CAS 67488-46-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.19 g/mol
Formula C₆H₈O₂S
badge Registry Numbers
MDL Number MFCD04038417
thermostat Physical Properties
Melting Point 34.0-38.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for functionalization that can enhance binding affinity to specific receptors. Commonly employed in medicinal chemistry for constructing heterocyclic compounds with biological activity. Also utilized in agrochemical research for designing new pesticides due to its reactive scaffold. Serves as a building block in organic synthesis, enabling the formation of complex thiophene derivatives with potential applications in materials science, including conductive polymers and organic electronics.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿700.00
inventory 1g
10-20 days ฿3,180.00
Methyl 2,5-Dihydrothiophene-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for functionalization that can enhance binding affinity to specific receptors. Commonly employed in medicinal chemistry for constructing heterocyclic compounds with biological activity. Also utilized in agrochemical research for designing new pesticides due to its reactive scaffold. Serves as a building block in organic synthesis, enabli

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. Its structure allows for functionalization that can enhance binding affinity to specific receptors. Commonly employed in medicinal chemistry for constructing heterocyclic compounds with biological activity. Also utilized in agrochemical research for designing new pesticides due to its reactive scaffold. Serves as a building block in organic synthesis, enabling the formation of complex thiophene derivatives with potential applications in materials science, including conductive polymers and organic electronics.

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