4-((2-methyl-5-nitrophenyl)sulfonyl)morpholine

≥95%

Reagent Code: #214235
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CAS Number 91215-03-1

science Other reagents with same CAS 91215-03-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.3 g/mol
Formula C₁₁H₁₄N₂O₅S
badge Registry Numbers
MDL Number MFCD00844666
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs. It serves as a building block in medicinal chemistry for creating biologically active molecules with potential antimicrobial and anti-inflammatory properties. Its structure allows for easy modification, making it valuable in optimizing drug candidates during research and development. Also employed in the preparation of enzyme inhibitors due to the electron-withdrawing nitro group and the conformational stability provided by the morpholine ring.

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inventory 1g
10-20 days ฿38,000.00

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4-((2-methyl-5-nitrophenyl)sulfonyl)morpholine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs. It serves as a building block in medicinal chemistry for creating biologically active molecules with potential antimicrobial and anti-inflammatory properties. Its structure allows for easy modification, making it valuable in optimizing drug candidates during research and development. Also employed in the preparation of enzyme inhibitors due to the electron-withdrawing nitro gr

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of sulfonamide-based drugs. It serves as a building block in medicinal chemistry for creating biologically active molecules with potential antimicrobial and anti-inflammatory properties. Its structure allows for easy modification, making it valuable in optimizing drug candidates during research and development. Also employed in the preparation of enzyme inhibitors due to the electron-withdrawing nitro group and the conformational stability provided by the morpholine ring.

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