Cas no 89850-95-3 (N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine)

N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine is a tertiary amine compound featuring a pyrrolidine scaffold with dual methyl substitutions. Its structural configuration imparts notable steric and electronic properties, making it a versatile intermediate in organic synthesis and pharmaceutical research. The compound's rigid pyrrolidine core enhances conformational stability, while the N-methyl groups influence its basicity and solubility profile. These characteristics render it suitable for applications in ligand design, catalysis, and the development of bioactive molecules. Its well-defined stereochemistry further allows for precise modulation in chiral synthesis. The compound is typically handled under inert conditions due to its sensitivity to moisture and air.
N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine structure
89850-95-3 structure
Product Name:N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine
CAS No:89850-95-3
MF:C7H16N2
MW:128.215341567993
MDL:MFCD07643216
CID:1006050
PubChem ID:15021556
Update Time:2025-11-06

N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine Chemical and Physical Properties

Names and Identifiers

    • N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine
    • N-methyl(1-methylpyrrolidin-3-yl)methanamine
    • 1-methyl-3-(methylamino)methylpyrrolidine
    • methyl[(1-methylpyrrolidin-3-yl)methyl]amine
    • rac-methyl-(1-methyl-pyrrolidin-3-ylmethyl)-amine
    • 1-Methyl-3-[(methylamino)methyl]pyrrolidine
    • BS-23923
    • Z594498314
    • EN300-69741
    • N-Methyl-1-(1-methyl-3-pyrrolidinyl)methanamine
    • ASINEX-REAG BAS 10144681
    • AM20120299
    • MFCD07643216
    • 89850-95-3
    • Methyl-(1-methyl-pyrrolidin-3-ylmethyl)-amine
    • CS-0204952
    • SCHEMBL90794
    • AKOS005174055
    • DTXSID40567081
    • G27602
    • ALBB-013302
    • MDL： MFCD07643216
    • Inchi： 1S/C7H16N2/c1-8-5-7-3-4-9(2)6-7/h7-8H,3-6H2,1-2H3
    • InChI Key： ZLDWGNZSKNMPRQ-UHFFFAOYSA-N
    • SMILES： N1(C)CCC(CNC)C1

Computed Properties

  • Exact Mass: 128.13100
  • Monoisotopic Mass: 128.131348519g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 2
  • Complexity: 83
  • 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: 0.2
  • Topological Polar Surface Area: 15.3?2

Experimental Properties

  • Density: 0.877
  • Boiling Point: 152 oC
  • Flash Point: 39 oC
  • Refractive Index: 1.454
  • PSA: 15.27000
  • LogP: 0.48630

N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine Customs Data

  • HS CODE：2933990090
  • Customs Data：

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine Pricemore >>

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N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine Related Literature

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Additional information on N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine

N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine: A Comprehensive Overview

N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine, also known by its CAS number 89850-95-3, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound has garnered attention due to its unique structural properties and potential applications in drug development. The molecule consists of a methanamine backbone with a methyl group attached to the nitrogen atom, further substituted by a 1-methylpyrrolidin-3-yl group. This combination of functional groups imparts distinctive chemical and biological characteristics to the compound.

Recent studies have highlighted the importance of N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine in the context of its role as a building block for more complex molecules. Researchers have explored its reactivity under various synthetic conditions, revealing its potential as an intermediate in the synthesis of bioactive compounds. The compound's ability to undergo nucleophilic substitution and other transformations makes it a valuable precursor in organic synthesis.

One of the most intriguing aspects of N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine is its interaction with biological systems. Preclinical studies have demonstrated that this compound exhibits moderate activity against certain enzymes, suggesting its potential as a lead compound for drug discovery. However, further research is required to fully understand its pharmacokinetic properties and safety profile.

The structural flexibility of N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine also lends itself to applications in materials science. Its ability to form stable complexes with metal ions has been explored in the context of catalysis and coordination chemistry. This versatility underscores the compound's importance across multiple disciplines.

In terms of synthesis, N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine can be prepared through a variety of methods, including nucleophilic substitution reactions and organocatalytic processes. These methods have been optimized to improve yield and purity, making the compound more accessible for research and development purposes.

Looking ahead, the continued exploration of N-Methyl-1-(1-methylpyrrolidin-3-yl)methanamine's properties is expected to yield further insights into its potential applications. As research progresses, this compound may play a pivotal role in advancing our understanding of complex chemical systems and their interactions with biological targets.

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