5,6-Dihydro-4-hydroxy-6-methyl-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-Dioxide

95%

Reagent Code: #178220
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CAS Number 120279-26-7

science Other reagents with same CAS 120279-26-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.37 g/mol
Formula C₈H₁₁NO₅S₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of carbonic anhydrase inhibitors, particularly in the production of dorzolamide, a topical ophthalmic agent for the treatment of glaucoma. It serves as the core scaffold in pharmaceutical manufacturing, enabling the formation of sulfonamide-based drugs that reduce intraocular pressure by inhibiting aqueous humor secretion in the eye. The sulfonamide group and bicyclic thieno[2,3-b]thiopyran framework are essential for potent enzyme inhibition and biological activity. Commonly utilized in controlled synthetic reactions to ensure high purity and yield in active pharmaceutical ingredient (API) production.

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5mg
10-20 days ฿6,420.00

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5,6-Dihydro-4-hydroxy-6-methyl-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-Dioxide
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Used as a key intermediate in the synthesis of carbonic anhydrase inhibitors, particularly in the production of dorzolamide, a topical ophthalmic agent for the treatment of glaucoma. It serves as the core scaffold in pharmaceutical manufacturing, enabling the formation of sulfonamide-based drugs that reduce intraocular pressure by inhibiting aqueous humor secretion in the eye. The sulfonamide group and bicyclic thieno[2,3-b]thiopyran framework are essential for potent enzyme inhibition and biological act

Used as a key intermediate in the synthesis of carbonic anhydrase inhibitors, particularly in the production of dorzolamide, a topical ophthalmic agent for the treatment of glaucoma. It serves as the core scaffold in pharmaceutical manufacturing, enabling the formation of sulfonamide-based drugs that reduce intraocular pressure by inhibiting aqueous humor secretion in the eye. The sulfonamide group and bicyclic thieno[2,3-b]thiopyran framework are essential for potent enzyme inhibition and biological activity. Commonly utilized in controlled synthetic reactions to ensure high purity and yield in active pharmaceutical ingredient (API) production.

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