2-Bromo-5-(N-Boc-piperidin-3-yl)thiophene

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Reagent Code: #43269
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CAS Number 1622834-60-9

science Other reagents with same CAS 1622834-60-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 346.2831 g/mol
Formula C₁₄H₂₀BrNO₂S
thermostat Physical Properties
Boiling Point 396.5±42.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.360±0.06 g/cm3
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the construction of complex molecules, especially those targeting therapeutic applications. The Boc (tert-butoxycarbonyl) group provides protection for the piperidine nitrogen during synthetic processes, allowing for selective reactions at other sites of the molecule. Its thiophene moiety is often employed in the design of drug candidates due to its bioisosteric properties, which can enhance binding affinity and metabolic stability. This compound is particularly relevant in the synthesis of small-molecule inhibitors and bioactive compounds for research in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,784.00
inventory 1g
10-20 days ฿38,592.00
inventory 250mg
10-20 days ฿14,652.00

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2-Bromo-5-(N-Boc-piperidin-3-yl)thiophene
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This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the construction of complex molecules, especially those targeting therapeutic applications. The Boc (tert-butoxycarbonyl) group provides protection for the piperidine nitrogen during synthetic processes, allowing for selective reactions at other sites of the molecule. Its thiophene moiety is often employed in the design of drug candidates due to its bio

This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the construction of complex molecules, especially those targeting therapeutic applications. The Boc (tert-butoxycarbonyl) group provides protection for the piperidine nitrogen during synthetic processes, allowing for selective reactions at other sites of the molecule. Its thiophene moiety is often employed in the design of drug candidates due to its bioisosteric properties, which can enhance binding affinity and metabolic stability. This compound is particularly relevant in the synthesis of small-molecule inhibitors and bioactive compounds for research in medicinal chemistry.

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