3-Oxetanyl p-toluenesulfonate

98%

Reagent Code: #221553
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CAS Number 26272-83-3

science Other reagents with same CAS 26272-83-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.27 g/mol
Formula C₁₀H₁₂O₄S
badge Registry Numbers
MDL Number MFCD08544401
thermostat Physical Properties
Boiling Point 372°C
inventory_2 Storage & Handling
Density 1.34g/mL
Storage Room temperature, dry

description Product Description

Used primarily as a reactive intermediate in organic synthesis, this compound enables the introduction of the 3-oxetanyl group into various molecules, taking advantage of its strained ring structure for ring-opening reactions. Its tosylate leaving group facilitates nucleophilic substitution under mild conditions, making it valuable in pharmaceutical synthesis where oxetane motifs can improve metabolic stability, solubility, and binding affinity of drug candidates. It is also employed in the preparation of functionalized building blocks for medicinal chemistry and in the development of agrochemicals and specialty materials requiring specific reactivity or structural features.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿320.00
5g
10-20 days ฿720.00
25g
10-20 days ฿2,430.00
3-Oxetanyl p-toluenesulfonate
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Used primarily as a reactive intermediate in organic synthesis, this compound enables the introduction of the 3-oxetanyl group into various molecules, taking advantage of its strained ring structure for ring-opening reactions. Its tosylate leaving group facilitates nucleophilic substitution under mild conditions, making it valuable in pharmaceutical synthesis where oxetane motifs can improve metabolic stability, solubility, and binding affinity of drug candidates. It is also employed in the preparation o

Used primarily as a reactive intermediate in organic synthesis, this compound enables the introduction of the 3-oxetanyl group into various molecules, taking advantage of its strained ring structure for ring-opening reactions. Its tosylate leaving group facilitates nucleophilic substitution under mild conditions, making it valuable in pharmaceutical synthesis where oxetane motifs can improve metabolic stability, solubility, and binding affinity of drug candidates. It is also employed in the preparation of functionalized building blocks for medicinal chemistry and in the development of agrochemicals and specialty materials requiring specific reactivity or structural features.

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