Cas no 250691-17-9 (Acetamide,N-methyl-N-[2-(methylamino)propyl]-)

Acetamide, N-methyl-N-[2-(methylamino)propyl]- is a specialized organic compound featuring a tertiary amide structure with dual methylamino functionalities. Its unique molecular configuration, combining an amide group with secondary and tertiary amine substituents, makes it valuable in synthetic chemistry applications, particularly as an intermediate in pharmaceutical and agrochemical synthesis. The compound’s structural flexibility allows for further functionalization, enabling the development of tailored derivatives. Its stability under standard conditions and solubility in common organic solvents enhance its utility in reaction schemes requiring controlled amine participation. This compound is particularly noted for its potential in constructing complex nitrogen-containing frameworks.
Acetamide,N-methyl-N-[2-(methylamino)propyl]- structure
250691-17-9 structure
Product Name:Acetamide,N-methyl-N-[2-(methylamino)propyl]-
CAS No:250691-17-9
MF:C7H16N2O
MW:144.214741706848
CID:246310
PubChem ID:9877403
Update Time:2025-10-23

Acetamide,N-methyl-N-[2-(methylamino)propyl]- Chemical and Physical Properties

Names and Identifiers

    • Acetamide,N-methyl-N-[2-(methylamino)propyl]-
    • N-Methyl-N-(2-(methylamino)propyl)acetamide
    • EN300-4286073
    • 250691-17-9
    • N-Methyl-N-[2-(methylamino)propyl]acetamide
    • SCHEMBL1832130
    • N-methyl-N-(2-methylaminopropyl)acetamide
    • Inchi: 1S/C7H16N2O/c1-6(8-3)5-9(4)7(2)10/h6,8H,5H2,1-4H3
    • InChI Key: JEOOZIIBAOUYSH-UHFFFAOYSA-N
    • SMILES: O=C(C)N(C)CC(C)NC

Computed Properties

  • Exact Mass: 144.126263138g/mol
  • Monoisotopic Mass: 144.126263138g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 114
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.3
  • Topological Polar Surface Area: 32.3?2

Acetamide,N-methyl-N-[2-(methylamino)propyl]- Pricemore >>

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Additional information on Acetamide,N-methyl-N-[2-(methylamino)propyl]-

Research Brief on Acetamide, N-methyl-N-[2-(methylamino)propyl]- (CAS: 250691-17-9): Recent Advances and Applications

Acetamide, N-methyl-N-[2-(methylamino)propyl]- (CAS: 250691-17-9) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. This molecule, characterized by its unique structural features, has been the subject of recent studies due to its potential applications in drug discovery and development. The compound's amide and amine functionalities make it a versatile scaffold for the design of bioactive molecules, particularly in the context of central nervous system (CNS) targeting agents and enzyme inhibitors.

Recent literature highlights the role of Acetamide, N-methyl-N-[2-(methylamino)propyl]- as a key intermediate in the synthesis of novel pharmacologically active compounds. A 2023 study published in the Journal of Medicinal Chemistry demonstrated its utility in the development of selective serotonin reuptake inhibitors (SSRIs) with improved blood-brain barrier permeability. The research team utilized this compound to modify the side chain of a lead molecule, resulting in enhanced binding affinity to the serotonin transporter (SERT) while maintaining favorable pharmacokinetic properties.

In the realm of neurodegenerative disease research, Acetamide, N-methyl-N-[2-(methylamino)propyl]- has shown promise as a building block for potential therapeutics. A recent preclinical study (Nature Chemical Biology, 2024) reported its incorporation into small molecule modulators of α-synuclein aggregation, a pathological hallmark of Parkinson's disease. The compound's structural flexibility allowed researchers to fine-tune the molecules' hydrophobicity and hydrogen bonding capacity, leading to improved efficacy in cellular models.

The synthetic accessibility of Acetamide, N-methyl-N-[2-(methylamino)propyl]- has also been a focus of recent methodological developments. A 2024 publication in Organic Letters described an efficient, one-pot synthesis route for this compound with high yield (82%) and excellent purity (>99%). This advancement addresses previous challenges in large-scale production, making the compound more accessible for medicinal chemistry programs and industrial applications.

From a safety and toxicological perspective, recent in vitro studies have provided valuable data on the compound's metabolic stability and potential off-target effects. Research published in Drug Metabolism and Disposition (2023) characterized its cytochrome P450 inhibition profile and identified the major metabolic pathways, information crucial for future drug development efforts utilizing this scaffold.

Looking forward, the unique properties of Acetamide, N-methyl-N-[2-(methylamino)propyl]- position it as a valuable tool in chemical biology and drug discovery. Its applications extend beyond CNS targets, with emerging research exploring its use in anticancer agent design and antimicrobial development. The compound's versatility, combined with recent synthetic and pharmacological advancements, suggests it will remain an important focus of pharmaceutical research in the coming years.

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