4-Thiomorpholinecarbonyl chloride, 1,1-dioxide

95%

Reagent Code: #242011
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CAS Number 39093-77-1

science Other reagents with same CAS 39093-77-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 197.64 g/mol
Formula C₅H₈ClNO₃S
badge Registry Numbers
MDL Number MFCD23790154
thermostat Physical Properties
Boiling Point 453.6±34.0 °C
inventory_2 Storage & Handling
Density 1.517±0.06 g/cm3
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It reacts readily with amines to form amide derivatives, making it valuable in constructing bioactive molecules. Commonly employed in the development of enzyme inhibitors and medicinal agents where the sulfonamide or sulfonyl carbonyl group enhances metabolic stability and binding affinity. Its cyclic sulfone structure contributes to improved solubility and conformational rigidity in final products, beneficial for drug design. Also utilized in peptide mimetics and heterocyclic chemistry to introduce functionalized rings that modulate pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,620.00
inventory 250mg
10-20 days ฿2,750.00
inventory 1g
10-20 days ฿7,430.00

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4-Thiomorpholinecarbonyl chloride, 1,1-dioxide
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It reacts readily with amines to form amide derivatives, making it valuable in constructing bioactive molecules. Commonly employed in the development of enzyme inhibitors and medicinal agents where the sulfonamide or sulfonyl carbonyl group enhances metabolic stability and binding affinity. Its cyclic sulfone structure contributes to improved solubility and conformational rigidity in final produc

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceutical compounds. It reacts readily with amines to form amide derivatives, making it valuable in constructing bioactive molecules. Commonly employed in the development of enzyme inhibitors and medicinal agents where the sulfonamide or sulfonyl carbonyl group enhances metabolic stability and binding affinity. Its cyclic sulfone structure contributes to improved solubility and conformational rigidity in final products, beneficial for drug design. Also utilized in peptide mimetics and heterocyclic chemistry to introduce functionalized rings that modulate pharmacokinetic properties.

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