tert-Butyl 3-iodopiperidine-1-carboxylate

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Reagent Code: #145537
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CAS Number 850761-36-3

science Other reagents with same CAS 850761-36-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.16 g/mol
Formula C₁₀H₁₈INO₂
badge Registry Numbers
MDL Number MFCD08059309
thermostat Physical Properties
Boiling Point 361.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. The presence of both iodine and a protected amine group makes it valuable for coupling reactions, such as Suzuki or Buchwald–Hartwig aminations, enabling the construction of complex piperidine-based structures. Commonly employed in medicinal chemistry for modifying pharmacokinetic properties or enhancing binding affinity in target compounds. Also utilized in the synthesis of agrochemicals and functionalized heterocycles.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿940.00
inventory 250mg
10-20 days ฿2,880.00

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tert-Butyl 3-iodopiperidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. The presence of both iodine and a protected amine group makes it valuable for coupling reactions, such as Suzuki or Buchwald–Hartwig aminations, enabling the construction of complex piperidine-based structures. Commonly employed in medicinal chemistry for modifying pharmacokinetic properties or enhancing binding affinity in target compounds. Also utilized in the synthesis of ag

Used as an intermediate in pharmaceutical synthesis, particularly in the development of bioactive molecules and drug candidates. The presence of both iodine and a protected amine group makes it valuable for coupling reactions, such as Suzuki or Buchwald–Hartwig aminations, enabling the construction of complex piperidine-based structures. Commonly employed in medicinal chemistry for modifying pharmacokinetic properties or enhancing binding affinity in target compounds. Also utilized in the synthesis of agrochemicals and functionalized heterocycles.

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