1-Benzoylpiperidine

98%

Reagent Code: #147287
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CAS Number 776-75-0

science Other reagents with same CAS 776-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.26 g/mol
Formula C₁₂H₁₅NO
badge Registry Numbers
MDL Number MFCD00023702
thermostat Physical Properties
Boiling Point 321°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a building block in the development of active pharmaceutical ingredients (APIs), leveraging its amide and aromatic functionalities to form new carbon-nitrogen or carbon-carbon bonds. Its structure is useful in medicinal chemistry for modifying pharmacokinetic properties or enhancing binding affinity in drug candidates. Also employed in research settings for exploring new synthetic pathways or as a protecting group strategy due to the stability of the piperidine ring.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿320.00
inventory 1g
10-20 days ฿1,540.00
inventory 5g
10-20 days ฿4,130.00
inventory 25g
10-20 days ฿20,280.00
inventory 100g
10-20 days ฿73,380.00

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1-Benzoylpiperidine
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a building block in the development of active pharmaceutical ingredients (APIs), leveraging its amide and aromatic functionalities to form new carbon-nitrogen or carbon-carbon bonds. Its structure is useful in medicinal chemistry for modifying pharmacokinetic properties or enhancing binding affinity in drug candidates. Also employed in research settings for exploring

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. It serves as a building block in the development of active pharmaceutical ingredients (APIs), leveraging its amide and aromatic functionalities to form new carbon-nitrogen or carbon-carbon bonds. Its structure is useful in medicinal chemistry for modifying pharmacokinetic properties or enhancing binding affinity in drug candidates. Also employed in research settings for exploring new synthetic pathways or as a protecting group strategy due to the stability of the piperidine ring.

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