1-(Thiophen-2-ylsulfonyl)piperidine-4-carboxylic acid

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Reagent Code: #238390
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CAS Number 327971-19-7

science Other reagents with same CAS 327971-19-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.35 g/mol
Formula C₁₀H₁₃NO₄S₂
badge Registry Numbers
MDL Number MFCD01925604
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective enzyme inhibitors and receptor antagonists. Its structure supports the design of bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing lead compounds in drug discovery programs targeting central nervous system disorders and inflammatory conditions. The sulfonyl and carboxylic acid functional groups allow for versatile derivatization, facilitating the preparation of amides and esters to fine-tune pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,280.00
inventory 1g
10-20 days ฿19,650.00
inventory 5g
10-20 days ฿68,770.00
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1-(Thiophen-2-ylsulfonyl)piperidine-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective enzyme inhibitors and receptor antagonists. Its structure supports the design of bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing lead compounds in drug discovery programs targeting central nervous system disorders and inflammatory conditions. The sulfonyl and carboxylic acid functional groups allow for versat

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective enzyme inhibitors and receptor antagonists. Its structure supports the design of bioactive molecules with improved metabolic stability and binding affinity. Commonly employed in medicinal chemistry for optimizing lead compounds in drug discovery programs targeting central nervous system disorders and inflammatory conditions. The sulfonyl and carboxylic acid functional groups allow for versatile derivatization, facilitating the preparation of amides and esters to fine-tune pharmacokinetic properties.

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