(S)-benzyl-[2-[(6-nitrobenzo[d]thiazol-2-yl)carbamoyl]pyrrolidine-1-yl]carboxylate

Reagent Code: #233610
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CAS Number 1848983-11-8

science Other reagents with same CAS 1848983-11-8

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Weight 426.453 g/mol
Formula C₂₀H₁₈N₄O₅S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of enzyme inhibitors. Its structure supports binding to specific protein targets, making it valuable in medicinal chemistry for designing drugs targeting inflammatory and neurodegenerative diseases. Also employed in research settings to develop fluorescent probes due to the nitrobenzothiazole moiety, which can be modified for detection in cellular imaging. Commonly applied in structure-activity relationship (SAR) studies to optimize potency and selectivity of drug candidates.

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inventory 1g
10-20 days ฿22,800.00

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(S)-benzyl-[2-[(6-nitrobenzo[d]thiazol-2-yl)carbamoyl]pyrrolidine-1-yl]carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of enzyme inhibitors. Its structure supports binding to specific protein targets, making it valuable in medicinal chemistry for designing drugs targeting inflammatory and neurodegenerative diseases. Also employed in research settings to develop fluorescent probes due to the nitrobenzothiazole moiety, which can be modified for detection in cellular imaging. Commonly applied in structure-activity rela

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of enzyme inhibitors. Its structure supports binding to specific protein targets, making it valuable in medicinal chemistry for designing drugs targeting inflammatory and neurodegenerative diseases. Also employed in research settings to develop fluorescent probes due to the nitrobenzothiazole moiety, which can be modified for detection in cellular imaging. Commonly applied in structure-activity relationship (SAR) studies to optimize potency and selectivity of drug candidates.

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