Cas no 1220038-27-6 (N,N-Dipropyl-3-pyrrolidinamine dihydrochloride)

N,N-Dipropyl-3-pyrrolidinamine dihydrochloride is a tertiary amine derivative with a pyrrolidine core structure, commonly utilized in pharmaceutical and chemical research. Its dihydrochloride salt form enhances stability and solubility, making it suitable for experimental applications requiring precise dosing. The compound's propyl substituents contribute to its lipophilicity, which can influence pharmacokinetic properties in drug development studies. As a building block, it serves in the synthesis of more complex molecules, particularly in central nervous system (CNS) research. The hydrochloride salt ensures consistent handling and storage characteristics, while its well-defined structure allows for reproducibility in synthetic workflows. This compound is typically employed under controlled laboratory conditions for specialized investigations.
N,N-Dipropyl-3-pyrrolidinamine dihydrochloride structure
1220038-27-6 structure
Product Name:N,N-Dipropyl-3-pyrrolidinamine dihydrochloride
CAS No:1220038-27-6
MF:C10H24Cl2N2
MW:243.216960906982
CID:1078494
PubChem ID:53410676
Update Time:2025-11-01

N,N-Dipropyl-3-pyrrolidinamine dihydrochloride Chemical and Physical Properties

Names and Identifiers

    • N,N-Dipropyl-3-pyrrolidinamine dihydrochloride
    • N,N-dipropylpyrrolidin-3-amine;dihydrochloride
    • N,N-dipropylpyrrolidin-3-aminedihydrochloride
    • AKOS015845388
    • 1220038-27-6
    • N,N-dipropylpyrrolidin-3-amine dihydrochloride
    • MDL: MFCD13561596
    • Inchi: 1S/C10H22N2.2ClH/c1-3-7-12(8-4-2)10-5-6-11-9-10;;/h10-11H,3-9H2,1-2H3;2*1H
    • InChI Key: ZRTGNIRTQLWVCF-UHFFFAOYSA-N
    • SMILES: Cl.Cl.N(CCC)(CCC)C1CNCC1

Computed Properties

  • Exact Mass: 242.1316542g/mol
  • Monoisotopic Mass: 242.1316542g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 5
  • Complexity: 108
  • 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

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N,N-Dipropyl-3-pyrrolidinamine dihydrochloride Related Literature

Additional information on N,N-Dipropyl-3-pyrrolidinamine dihydrochloride

N,N-Dipropyl-3-pyrrolidinamine Dihydrochloride (CAS No. 1220038-27-6)

N,N-Dipropyl-3-pyrrolidinamine dihydrochloride is a chemical compound with the CAS registry number 1220038-27-6. This compound belongs to the class of pyrrolidinamines, which are derivatives of pyrrolidine, a five-membered saturated heterocyclic amine. The structure of this compound consists of a pyrrolidine ring with an amine group at the 3-position and two propyl groups attached to the nitrogen atom. The dihydrochloride form indicates that the compound is in its hydrochloride salt form, which is commonly used in pharmaceutical and chemical applications.

The synthesis of N,N-Dipropyl-3-pyrrolidinamine dihydrochloride typically involves the reaction of 3-pyrrolidinamine with propylating agents in the presence of an acid catalyst. The dihydrochloride salt is often formed during the workup process, where the free base is treated with hydrochloric acid to yield the salt. This compound is known for its stability and solubility properties, making it suitable for various applications in organic synthesis and drug development.

Recent studies have highlighted the potential of N,N-Dipropyl-3-pyrrolidinamine dihydrochloride as a precursor or intermediate in the synthesis of bioactive molecules. For instance, researchers have explored its use in the development of novel antiviral agents, where its unique structure allows for interactions with viral proteins or enzymes. Additionally, this compound has been investigated for its role in modulating cellular signaling pathways, particularly those involved in inflammation and neurodegenerative diseases.

In terms of pharmacological applications, N,N-Dipropyl-3-pyrrolidinamine dihydrochloride has shown promise as a potential drug candidate due to its ability to cross cellular membranes and interact with intracellular targets. Preclinical studies have demonstrated its efficacy in reducing oxidative stress and inhibiting pro-inflammatory cytokines, suggesting its potential utility in treating conditions such as arthritis and neuroinflammation.

The structural versatility of N,N-Dipropyl-3-pyrrolidinamine dihydrochloride also makes it an attractive substrate for further chemical modifications. For example, researchers have employed this compound as a starting material for synthesizing more complex molecules with enhanced bioactivity. By introducing additional functional groups or modifying the existing substituents, scientists can tailor the properties of this compound to suit specific therapeutic needs.

In conclusion, N,N-Dipropyl-3-pyrrolidinamine dihydrochloride (CAS No. 1220038-27-6) is a valuable compound with diverse applications in organic synthesis and drug discovery. Its unique structure, coupled with favorable physicochemical properties, positions it as a promising candidate for developing novel therapeutic agents. Ongoing research continues to uncover new insights into its potential uses, further solidifying its importance in the field of medicinal chemistry.

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