4-(3-Aminopropyl)thiomorpholine 1,1-Dioxide

≥98%

Reagent Code: #136325
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CAS Number 90000-25-2

science Other reagents with same CAS 90000-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.28 g/mol
Formula C₇H₁₆N₂O₂S
thermostat Physical Properties
Boiling Point 190°C/0.6mmHg(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a building block in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its amine and sulfone functional groups make it suitable for use in cross-coupling reactions and as a linker in drug design. Commonly employed in the synthesis of kinase inhibitors and other therapeutic agents where a polar, flexible spacer is required. Also utilized in the preparation of ligands for receptor binding studies due to its ability to mimic certain peptide motifs.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,380.00
inventory 1g
10-20 days ฿4,450.00

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4-(3-Aminopropyl)thiomorpholine 1,1-Dioxide
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Used as a building block in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its amine and sulfone functional groups make it suitable for use in cross-coupling reactions and as a linker in drug design. Commonly employed in the synthesis of kinase inhibitors and other therapeutic agents where a polar, flexible spacer is required. Also utilized in the preparation of ligands for receptor binding studies due to its ability to mimic certain peptide motifs.
Used as a building block in organic synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its amine and sulfone functional groups make it suitable for use in cross-coupling reactions and as a linker in drug design. Commonly employed in the synthesis of kinase inhibitors and other therapeutic agents where a polar, flexible spacer is required. Also utilized in the preparation of ligands for receptor binding studies due to its ability to mimic certain peptide motifs.
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