1-(3-Methoxy-4-nitrophenyl)piperidin-4-one

97%

Reagent Code: #209565
fingerprint
CAS Number 761440-64-6

science Other reagents with same CAS 761440-64-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.25 g/mol
Formula C₁₂H₁₄N₂O₄
inventory_2 Storage & Handling
Storage Dry, 2-8℃

description Product Description

1-(3-Methoxy-4-nitrophenyl)piperidin-4-one is used primarily in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure, featuring a 3-methoxy-4-nitrophenyl group attached to a piperidin-4-one ring, supports derivatization for drug development, particularly in creating analogs with potential central nervous system activity due to the methoxy and nitro groups enhancing blood-brain barrier penetration and interactions with brain receptors. It is commonly employed in the preparation of nitroaromatic compounds that can be reduced to amines for further functionalization. Additionally, it is utilized in research settings to develop novel heterocyclic systems with potential antimicrobial or anti-inflammatory properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,920.00
5g
10-20 days ฿13,060.00
1-(3-Methoxy-4-nitrophenyl)piperidin-4-one
No image available

1-(3-Methoxy-4-nitrophenyl)piperidin-4-one is used primarily in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure, featuring a 3-methoxy-4-nitrophenyl group attached to a piperidin-4-one ring, supports derivatization for drug development, particularly in creating analogs with potential central nervous system activity due to the methoxy and nitro groups enhancing blood-brain barrier penetration and interactions with brain receptors. It is commonly employed in

1-(3-Methoxy-4-nitrophenyl)piperidin-4-one is used primarily in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure, featuring a 3-methoxy-4-nitrophenyl group attached to a piperidin-4-one ring, supports derivatization for drug development, particularly in creating analogs with potential central nervous system activity due to the methoxy and nitro groups enhancing blood-brain barrier penetration and interactions with brain receptors. It is commonly employed in the preparation of nitroaromatic compounds that can be reduced to amines for further functionalization. Additionally, it is utilized in research settings to develop novel heterocyclic systems with potential antimicrobial or anti-inflammatory properties.

Mechanism -
Appearance -
Longevity -
Strength -
Long-term 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...