1-Tosylpiperidine

≥95%

Reagent Code: #131002
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CAS Number 4703-22-4

science Other reagents with same CAS 4703-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.33 g/mol
Formula C₁₂H₁₇NO₂S
badge Registry Numbers
MDL Number MFCD00159367
thermostat Physical Properties
Melting Point 98 °C
Boiling Point 368.2±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.190±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It serves as a protected form of piperidine, allowing selective reactions at other sites in the molecule. Commonly employed in the synthesis of alkaloids, antipsychotics, and other nitrogen-containing heterocycles. Its tosyl group can be removed under mild conditions, making it valuable in multi-step synthetic routes. Also utilized in the development of agrochemicals and functional materials due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿13,300.00
inventory 250mg
10-20 days ฿4,930.00

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1-Tosylpiperidine
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It serves as a protected form of piperidine, allowing selective reactions at other sites in the molecule. Commonly employed in the synthesis of alkaloids, antipsychotics, and other nitrogen-containing heterocycles. Its tosyl group can be removed under mild conditions, making it valuable in multi-step synthetic routes. Also utilized in the development of agrochemicals and fun

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It serves as a protected form of piperidine, allowing selective reactions at other sites in the molecule. Commonly employed in the synthesis of alkaloids, antipsychotics, and other nitrogen-containing heterocycles. Its tosyl group can be removed under mild conditions, making it valuable in multi-step synthetic routes. Also utilized in the development of agrochemicals and functional materials due to its stability and reactivity profile.

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