4,5-Dihydro-7H-thieno[2,3-c]pyran-7-one

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Reagent Code: #180017
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CAS Number 28424-70-6

science Other reagents with same CAS 28424-70-6

blur_circular Chemical Specifications

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Weight 154.19 g/mol
Formula C₇H₆O₂S
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MDL Number MFCD26096701
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the development of pharmaceuticals, particularly in the construction of heterocyclic frameworks found in bioactive molecules. Its structure supports ring transformations and functionalization useful in drug discovery. It has been explored in the synthesis of central nervous system agents and anti-inflammatory compounds due to its ability to mimic pharmacophores in medicinal chemistry. Additionally, it acts as a building block in the preparation of fused thiophene derivatives, which show potential in materials science, including organic semiconductors and fluorescent probes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,600.00

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4,5-Dihydro-7H-thieno[2,3-c]pyran-7-one
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Used primarily as an intermediate in organic synthesis, this compound serves in the development of pharmaceuticals, particularly in the construction of heterocyclic frameworks found in bioactive molecules. Its structure supports ring transformations and functionalization useful in drug discovery. It has been explored in the synthesis of central nervous system agents and anti-inflammatory compounds due to its ability to mimic pharmacophores in medicinal chemistry. Additionally, it acts as a building block

Used primarily as an intermediate in organic synthesis, this compound serves in the development of pharmaceuticals, particularly in the construction of heterocyclic frameworks found in bioactive molecules. Its structure supports ring transformations and functionalization useful in drug discovery. It has been explored in the synthesis of central nervous system agents and anti-inflammatory compounds due to its ability to mimic pharmacophores in medicinal chemistry. Additionally, it acts as a building block in the preparation of fused thiophene derivatives, which show potential in materials science, including organic semiconductors and fluorescent probes.

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