Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate

95%

Reagent Code: #39213
fingerprint
CAS Number 318280-71-6

science Other reagents with same CAS 318280-71-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.7000 g/mol
Formula C₁₀H₁₆ClNO₃
badge Registry Numbers
MDL Number MFCD01480849
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring both a chloroacetyl group and a piperidine ring, makes it a versatile building block for designing compounds with potential therapeutic properties. It is often employed in the synthesis of analogs targeting neurological disorders, such as acetylcholinesterase inhibitors, which are used in the treatment of Alzheimer's disease. Additionally, it serves as a precursor in the development of compounds with potential anticancer, antimicrobial, or anti-inflammatory activities. Its reactivity allows for further functionalization, enabling researchers to explore diverse chemical modifications for drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,440.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 1-(2-chloroacetyl)piperidine-4-carboxylate
No image available
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various pharmaceuticals and bioactive molecules. Its structure, featuring both a chloroacetyl group and a piperidine ring, makes it a versatile building block for designing compounds with potential therapeutic properties. It is often employed in the synthesis of analogs targeting neurological disorders, such as acetylcholinesterase inhibitors, which are used in the treatment of Alzheimer's disease. Additionally, it serves as a precursor in the development of compounds with potential anticancer, antimicrobial, or anti-inflammatory activities. Its reactivity allows for further functionalization, enabling researchers to explore diverse chemical modifications for drug discovery and development.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...