Cas no 933701-05-4 ((1-Piperidin-1-ylcyclopentyl)methylamine)

(1-Piperidin-1-ylcyclopentyl)methylamine is a cyclic amine derivative featuring a piperidine-substituted cyclopentyl core with a methylamine functional group. This compound is of interest in medicinal chemistry and pharmaceutical research due to its structural versatility, which allows for potential applications as a building block in the synthesis of bioactive molecules. The piperidine moiety enhances binding affinity to certain biological targets, while the cyclopentyl scaffold contributes to conformational rigidity, improving selectivity. Its amine group provides a reactive site for further derivatization, making it valuable in drug discovery and development. The compound's stability and synthetic accessibility further underscore its utility in exploratory research and fine chemical applications.
(1-Piperidin-1-ylcyclopentyl)methylamine structure
933701-05-4 structure
Product Name:(1-Piperidin-1-ylcyclopentyl)methylamine
CAS No:933701-05-4
MF:C11H22N2
MW:182.305782794952
MDL:MFCD09055382
CID:802204
PubChem ID:24708164
Update Time:2025-06-28

(1-Piperidin-1-ylcyclopentyl)methylamine Chemical and Physical Properties

Names and Identifiers

    • Cyclopentanemethanamine,1-(1-piperidinyl)-
    • (1-piperidin-1-ylcyclopentyl)methanamine
    • (1-piperidin-1-ylcyclopentyl)methylamine
    • (1-piperidin-1-ylcyclopentyl)methylamine, AldrichCPR
    • 1-[1-(1-Piperidinyl)cyclopentyl]methanamine
    • CS-0319032
    • DTXSID80640948
    • FT-0678889
    • 1-[1-(piperidin-1-yl)cyclopentyl]methanamine
    • SB41470
    • AKOS000193143
    • MFCD09055382
    • SCHEMBL3930544
    • (1-(Piperidin-1-yl)cyclopentyl)methanamine
    • 1-(1-piperidin-1-ylcyclopentyl)methanamine
    • FS-4872
    • 933701-05-4
    • ALBB-000076
    • STK502195
    • (1-Piperidin-1-ylcyclopentyl)methylamine
    • MDL: MFCD09055382
    • Inchi: 1S/C11H22N2/c12-10-11(6-2-3-7-11)13-8-4-1-5-9-13/h1-10,12H2
    • InChI Key: KEDRZSDDGPZNTE-UHFFFAOYSA-N
    • SMILES: N1(CCCCC1)C1(CN)CCCC1

Computed Properties

  • Exact Mass: 182.17800
  • Monoisotopic Mass: 182.178298710g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 156
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.3
  • Topological Polar Surface Area: 29.3?2

Experimental Properties

  • Density: 0.995
  • Boiling Point: 235.1°C at 760 mmHg
  • Flash Point: 92.7°C
  • Refractive Index: 1.522
  • PSA: 29.26000
  • LogP: 2.38200
  • Vapor Pressure: 0.1±0.5 mmHg at 25°C

(1-Piperidin-1-ylcyclopentyl)methylamine Security Information

(1-Piperidin-1-ylcyclopentyl)methylamine Customs Data

  • HS CODE:2933399090
  • Customs Data:

    China Customs Code:

    2933399090

    Overview:

    2933399090. Other compounds with non fused pyridine rings in structure. 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:

    2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

(1-Piperidin-1-ylcyclopentyl)methylamine Pricemore >>

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(1-Piperidin-1-ylcyclopentyl)methylamine Related Literature

Additional information on (1-Piperidin-1-ylcyclopentyl)methylamine

The Compound CAS No. 933701-05-4: (1-Piperidin-1-ylcyclopentyl)methylamine

The compound with CAS No. 933701-05-4, commonly referred to as (1-Piperidin-1-ylcyclopentyl)methylamine, is a complex organic molecule that has garnered significant attention in the fields of organic chemistry and pharmacology. This compound is characterized by its unique structure, which combines a piperidine ring, a cyclopentane ring, and an amine group. The piperidine moiety is a six-membered ring containing one nitrogen atom, while the cyclopentane ring is a five-membered hydrocarbon. The methylamine group further adds to the compound's functional diversity, making it a versatile molecule for various applications.

Recent studies have highlighted the potential of (1-Piperidin-1-ylcyclopentyl)methylamine in drug discovery and development. Researchers have explored its ability to act as a precursor for more complex molecules or as an intermediate in synthetic pathways leading to bioactive compounds. The compound's structure allows for extensive modification, enabling scientists to tailor its properties for specific therapeutic applications. For instance, modifications to the piperidine or cyclopentane rings can influence the molecule's lipophilicity, solubility, and bioavailability, which are critical factors in drug design.

One of the most promising areas of research involving this compound is its role in the development of neuroprotective agents. Studies have shown that derivatives of (1-Piperidin-1-ylcyclopentyl)methylamine can interact with key neurotransmitter systems, potentially offering therapeutic benefits for neurodegenerative diseases such as Alzheimer's and Parkinson's. The compound's ability to modulate these systems without causing significant side effects has made it a valuable tool in preclinical studies.

In addition to its pharmacological applications, (1-Piperidin-1-ylcyclopentyl)methylamine has also been investigated for its role in materials science. Its unique structure makes it a candidate for use in the synthesis of advanced polymers and materials with tailored mechanical and electronic properties. Researchers have explored its potential as a building block for self-healing polymers and stimuli-responsive materials, which could revolutionize industries ranging from electronics to healthcare.

The synthesis of (1-Piperidin-1-ylcyclopentyl)methylamine involves a series of carefully controlled reactions that highlight the principles of modern organic chemistry. The process typically begins with the preparation of the piperidine ring, followed by its coupling with the cyclopentane moiety. The final step involves the introduction of the methylamine group, which requires precise control over reaction conditions to ensure optimal yields and purity. This multi-step synthesis underscores the importance of advanced chemical techniques in producing such complex molecules.

From an environmental perspective, researchers have also examined the biodegradability and ecological impact of (1-Piperidin-1-ylcyclopentyl)methylamine. Studies suggest that under certain conditions, the compound can undergo microbial degradation, reducing its persistence in the environment. However, further research is needed to fully understand its long-term effects on ecosystems and to develop strategies for minimizing any potential risks associated with its use.

In conclusion, (1-Piperidin-1-ylcyclopentyl)methylamine (CAS No. 933701-05-4) is a multifaceted compound with significant potential across various scientific disciplines. Its unique structure, coupled with recent advancements in synthetic and analytical techniques, positions it as a valuable tool in drug discovery, materials science, and environmental studies. As research continues to uncover new applications and properties of this compound, it is likely to play an increasingly important role in shaping future innovations across these fields.

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