110429-36-2 | N-Methylparoxetine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$72.00	$50.00
5g	98%	in stock	$209.00	$146.00
10g	98%	in stock	$316.00	$221.00
25g	98%	in stock	$602.00	$421.00

Description

• Catalog Number: AI68790
• Chemical Name: N-Methylparoxetine
• CAS Number: 110429-36-2
• Molecular Formula: C20H22FNO3
• Molecular Weight: 343.392
• MDL Number: MFCD03788781
• SMILES: CN1CC[C@H]([C@@H](C1)COc1ccc2c(c1)OCO2)c1ccc(cc1)F

Computed Properties

• Complexity: 429
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 25
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• XLogP3: 4

Upstream Synthesis Route

(3S,4R)-3-((Benzo[d][1,3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-1-methylpiperidine is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. This compound serves as a valuable building block for the creation of various pharmaceuticals and fine chemicals. With its precise stereochemistry and functional groups, it can be utilized as a key intermediate in the synthesis of complex organic molecules.In chemical synthesis, (3S,4R)-3-((Benzo[d][1,3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-1-methylpiperidine can be employed in the formation of novel drug candidates, agrochemicals, and materials. Its piperidine ring provides a stable scaffold for further modifications, enabling the introduction of diverse substituents to tailor the properties of the final product. The benzo[d][1,3]dioxole moiety offers additional flexibility for designing molecules with specific biological activities or physical characteristics.Researchers and synthetic chemists value the versatility of (3S,4R)-3-((Benzo[d][1,3]dioxol-5-yloxy)methyl)-4-(4-fluorophenyl)-1-methylpiperidine in their endeavors to create innovative compounds with potential therapeutic, agricultural, or industrial applications. By incorporating this compound into their synthetic routes, scientists can access a wide range of chemical space and explore new avenues for drug discovery and material science.

Literature

• Structural differences between paroxetine and femoxetine responsible for differential inhibition of Staphylococcus aureus efflux pumps.

  Bioorganic & medicinal chemistry letters 20040621