2-(6,7-Dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetic acid

≥95%

Reagent Code: #177297
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CAS Number 926248-27-3

science Other reagents with same CAS 926248-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.25 g/mol
Formula C₉H₁₁NO₂S
badge Registry Numbers
MDL Number MFCD09042600
inventory_2 Storage & Handling
Storage 2-8°C, inert gas storage

description Product Description

Used primarily in the synthesis of pharmaceutical intermediates, this compound plays a key role in the development of antimuscarinic drugs. It is notably involved in the production of solifenacin, a medication used to treat overactive bladder by relaxing the muscles in the bladder. Its structure allows for effective binding and selectivity towards muscarinic receptors, making it valuable in urological therapeutics. Additionally, due to its bicyclic heterocyclic backbone, it serves as a building block in medicinal chemistry for designing new bioactive molecules with improved pharmacokinetic profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,940.00
inventory 250mg
10-20 days ฿9,260.00

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2-(6,7-Dihydrothieno[3,2-c]pyridin-5(4H)-yl)acetic acid
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Used primarily in the synthesis of pharmaceutical intermediates, this compound plays a key role in the development of antimuscarinic drugs. It is notably involved in the production of solifenacin, a medication used to treat overactive bladder by relaxing the muscles in the bladder. Its structure allows for effective binding and selectivity towards muscarinic receptors, making it valuable in urological therapeutics. Additionally, due to its bicyclic heterocyclic backbone, it serves as a building block in

Used primarily in the synthesis of pharmaceutical intermediates, this compound plays a key role in the development of antimuscarinic drugs. It is notably involved in the production of solifenacin, a medication used to treat overactive bladder by relaxing the muscles in the bladder. Its structure allows for effective binding and selectivity towards muscarinic receptors, making it valuable in urological therapeutics. Additionally, due to its bicyclic heterocyclic backbone, it serves as a building block in medicinal chemistry for designing new bioactive molecules with improved pharmacokinetic profiles.

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