Cas no 1219960-73-2 (N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride)

N,N-Dimethyl-2-(3-piperidinyl)ethanamine dihydrochloride is a synthetic organic compound featuring a piperidine core substituted with a dimethylaminoethyl group, presented as its dihydrochloride salt for enhanced stability and solubility. This structure lends itself to applications in pharmaceutical research, particularly as a versatile intermediate in the synthesis of bioactive molecules. The dihydrochloride form ensures improved handling characteristics and compatibility with aqueous systems. Its well-defined chemical properties make it suitable for use in medicinal chemistry, where precise reactivity and purity are critical. The compound's structural features may also facilitate studies in receptor binding or enzyme modulation, depending on derivative functionalization.
N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride structure
1219960-73-2 structure
Product Name:N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride
CAS No:1219960-73-2
MF:C9H22Cl2N2
MW:229.190380573273
MDL:MFCD13561633
CID:1071954
PubChem ID:50944366
Update Time:2025-06-13

N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • N,N-Dimethyl-2-(3-piperidinyl)-1-ethanamine dihydrochloride
    • 1219960-73-2
    • N,N-Dimethyl-2-(piperidin-3-yl)ethanamine dihydrochloride
    • MFCD13561633
    • N,N-dimethyl-2-piperidin-3-ylethanamine;dihydrochloride
    • N,N-dimethyl-2-(piperidin-3-yl)ethan-1-amine dihydrochloride
    • N,N-Dimethyl-2-piperidin-3-ylethanamine dihydrochloride
    • AKOS015845588
    • N,N-Dimethyl-2-(piperidin-3-yl)ethanaminedihydrochloride
    • dimethyl[2-(piperidin-3-yl)ethyl]amine dihydrochloride
    • N,N-Dimethyl-2-piperidin-3-ylethanamine dihydrochloride, AldrichCPR
    • N,N-dimethyl-2-(3-piperidinyl)ethanamine dihydrochloride
    • BS-40899
    • CS-0362420
    • N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride
    • MDL: MFCD13561633
    • Inchi: 1S/C9H20N2.2ClH/c1-11(2)7-5-9-4-3-6-10-8-9;;/h9-10H,3-8H2,1-2H3;2*1H
    • InChI Key: ZXULICJZKAKIGT-UHFFFAOYSA-N
    • SMILES: Cl.Cl.N1CCCC(CCN(C)C)C1

Computed Properties

  • Exact Mass: 228.1160041g/mol
  • Monoisotopic Mass: 228.1160041g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 102
  • Covalently-Bonded Unit Count: 3
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 15.3?2

Experimental Properties

  • Color/Form: NA

N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride Security Information

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N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride Related Literature

Additional information on N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride

Comprehensive Overview of N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride (CAS No. 1219960-73-2)

N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride (CAS No. 1219960-73-2) is a chemically significant compound that has garnered attention in various research and industrial applications. This compound, often referred to by its systematic name, belongs to the class of tertiary amines and features a piperidine ring, which is a common structural motif in many bioactive molecules. The dihydrochloride salt form enhances its solubility and stability, making it a preferred choice for laboratory and experimental use.

The molecular structure of N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride includes a dimethylamino group attached to a piperidinyl backbone, which contributes to its unique physicochemical properties. Researchers have explored its potential in medicinal chemistry, particularly in the design of novel pharmacophores. Its ability to interact with biological targets has made it a subject of interest in drug discovery and neuroscience studies.

In recent years, the demand for high-purity chemical compounds like N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride has surged, driven by advancements in biotechnology and pharmaceutical research. Users often search for terms such as "piperidine derivatives," "amine-based compounds," and "CAS 1219960-73-2 applications," reflecting the growing curiosity about its uses. This compound is also frequently discussed in forums related to synthetic chemistry and molecular design, where professionals seek insights into its reactivity and potential applications.

One of the key advantages of N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride is its versatility. It serves as a valuable intermediate in the synthesis of more complex molecules, particularly those targeting central nervous system (CNS) disorders. Its lipophilic nature allows it to cross the blood-brain barrier, a critical feature for CNS-active compounds. This property has led to its inclusion in studies focusing on neurotransmitter modulation and receptor binding.

From a safety and handling perspective, N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride should be stored under controlled conditions to maintain its integrity. Proper laboratory protocols, including the use of personal protective equipment (PPE), are essential when working with this compound. Researchers often inquire about "CAS 1219960-73-2 solubility" and "stability under various pH conditions," highlighting the need for detailed technical data.

The synthesis of N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride involves multi-step organic reactions, often starting from readily available piperidine precursors. Optimizing the yield and purity of this compound requires expertise in organic synthesis techniques, such as reductive amination and salt formation. These processes are frequently discussed in academic literature and patent filings, underscoring the compound's relevance in industrial chemistry.

In the context of green chemistry, there is increasing interest in developing sustainable methods for producing compounds like N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride. Researchers are exploring catalytic processes and solvent-free reactions to minimize environmental impact. This aligns with broader trends in the chemical industry, where eco-friendly synthesis is a priority.

Looking ahead, the potential applications of N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride are likely to expand as new discoveries emerge. Its role in material science, particularly in the development of functional polymers, is an area of ongoing investigation. Additionally, its utility in analytical chemistry as a reference standard or reagent further underscores its importance.

For those seeking detailed information about CAS No. 1219960-73-2, reliable sources include peer-reviewed journals, chemical databases, and supplier catalogs. Keywords such as "N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride supplier" and "technical data sheet" are commonly used in searches, emphasizing the need for accurate and accessible information.

In summary, N,N-Dimethyl-2-(3-piperidinyl)ethanamine Dihydrochloride (CAS No. 1219960-73-2) is a compound of significant scientific and industrial interest. Its unique structure, combined with its diverse applications, makes it a valuable tool for researchers and chemists worldwide. As the field of chemical innovation continues to evolve, this compound is poised to play a pivotal role in shaping future advancements.

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