Cas no 67907-32-8 (2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine)

2-(Aminomethyl)-3,3,5-trimethylcyclopentan-1-amine is a bicyclic amine compound featuring both primary and secondary amine functionalities. Its unique sterically hindered structure, with three methyl groups and a cyclopentane backbone, enhances its utility as a versatile intermediate in organic synthesis. The dual amine groups enable its use in chelation, catalysis, and the preparation of specialty polymers or pharmaceuticals. The compound’s rigid cyclic framework contributes to improved thermal and chemical stability, making it suitable for applications requiring robust performance under demanding conditions. Its reactivity can be tailored for selective modifications, offering flexibility in fine chemical and agrochemical synthesis.
2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine structure
67907-32-8 structure
Product Name:2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine
CAS No:67907-32-8
MF:C9H20N2
MW:156.268502235413
MDL:MFCD00001383
CID:967752
PubChem ID:106962
Update Time:2025-11-01

2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine Chemical and Physical Properties

Names and Identifiers

    • 5-amino-2,2,4-trimethyl-1-cyclopentanemethylamine
    • 5-AMINO-2,2,4-TRIMETHYL-1-CYCLOPENTANEMETHYLAMINE, MIXTURE OF ISOMERS,99
    • (1R,2R,5R)-2-(ammoniomethyl)-3,3,5-trimethylcyclopentanaminium
    • (1R,2R,5S)-2-(ammoniomethyl)-3,3,5-trimethylcyclopentanaminium
    • (1R,2S,5R)-2-(ammoniomethyl)-3,3,5-trimethylcyclopentanaminium
    • (1R,2S,5S)-2-(ammoniomethyl)-3,3,5-trimethylcyclopentanaminium
    • 2-(aminomethyl)-3,3,5-trimethylcyclopentanamine
    • 5-aminomethyl-2,4,4-trimethyl-1-cyclopentylamine
    • 2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine
    • DTXSID80887038
    • VS-13695
    • 5-amino-2,2,4-trimethylcyclopentylmethylamine
    • EN300-20925
    • Cyclopentanemethanamine, 5-amino-2,2,4-trimethyl-
    • CHEBI:229403
    • CS-0239307
    • 1-Amino-2-aminomethyl-3,3,5-trimethylcyclopentane
    • EINECS 267-741-1
    • 67907-32-8
    • AKOS000120745
    • 2-(Aminomethyl)-3,3,5-trimethylcyclopentanamine #
    • hexane-1,6-disulfonic acid- n-butyl-n-ethylbutan-1-amine(1:2)
    • SCHEMBL221846
    • MDL: MFCD00001383
    • Inchi: 1S/C9H20N2/c1-6-4-9(2,3)7(5-10)8(6)11/h6-8H,4-5,10-11H2,1-3H3
    • InChI Key: QKHWUKPTSMULMZ-UHFFFAOYSA-N
    • SMILES: NC1C(C)CC(C)(C)C1CN

Computed Properties

  • Exact Mass: 156.162648646g/mol
  • Monoisotopic Mass: 156.162648646g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 143
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 3
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.3
  • Topological Polar Surface Area: 52?2

Experimental Properties

  • Density: 0.9000
  • Boiling Point: 270.54°C (rough estimate)
  • Refractive Index: 1.4706 (estimate)

2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine Security Information

  • Hazardous Material transportation number:2735
  • HazardClass:8
  • PackingGroup:III
  • Safety Term:S24/25

2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine Pricemore >>

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Additional information on 2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine

Comprehensive Overview of 2-(Aminomethyl)-3,3,5-trimethylcyclopentan-1-amine (CAS No. 67907-32-8)

The compound 2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine (CAS No. 67907-32-8) is a specialized cyclopentane derivative with a unique amine-functionalized structure. Its molecular framework, featuring a trimethyl-substituted cyclopentane core, makes it a valuable intermediate in pharmaceutical synthesis and material science. Researchers and industries are increasingly interested in this compound due to its potential applications in bioactive molecule design and catalysis, aligning with current trends in green chemistry and sustainable manufacturing.

One of the most searched questions about CAS No. 67907-32-8 revolves around its synthetic routes and industrial scalability. Recent studies highlight its role as a chiral building block for asymmetric synthesis, a hot topic in drug discovery. The compound’s stereochemical complexity allows for the creation of enantiomerically pure compounds, addressing the growing demand for high-purity intermediates in API production. This aligns with the pharmaceutical industry’s shift toward precision medicine and personalized therapeutics.

From a structural-activity relationship perspective, the aminomethyl and amine groups in 2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine provide versatile sites for derivatization. This flexibility is critical for developing novel ligands in metal-organic frameworks (MOFs) or enzyme inhibitors, topics frequently explored in academic research and patent filings. Users searching for "amine-functionalized cyclopentane applications" or "CAS 67907-32-8 solubility data" often seek insights into its physicochemical properties, such as logP and hydrogen bonding capacity, which are essential for formulation development.

The compound’s relevance extends to agrochemical research, where its structural motifs are investigated for pest control agents. With rising global interest in eco-friendly pesticides, 67907-32-8 is occasionally referenced in studies exploring low-toxicity alternatives. Additionally, its thermal stability and compatibility with polymer matrices make it a candidate for advanced material engineering, particularly in epoxy resins and adhesive formulations—key areas in industrial adhesive searches.

Analytical methods for characterizing 2-(aminomethyl)-3,3,5-trimethylcyclopentan-1-amine, such as HPLC purity analysis and NMR spectroscopy, are frequently discussed in quality control forums. Laboratories prioritize method validation for this compound due to its regulatory significance in GMP compliance. Searches like "CAS 67907-32-8 spectroscopy data" reflect user needs for reference standards and technical documentation.

In summary, 67907-32-8 represents a multifaceted compound bridging pharmaceutical, material science, and agrochemical domains. Its synthetic versatility and functional group reactivity continue to inspire innovation, making it a subject of persistent interest in both academic and industrial settings.

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