Cas no 827614-53-9 (1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl-)

1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl- structure
827614-53-9 structure
Product Name:1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl-
CAS No:827614-53-9
MF:C14H31N3
MW:241.416043519974
MDL:MFCD03701085
CID:716012
PubChem ID:2758721
Update Time:2025-06-18

1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl- Chemical and Physical Properties

Names and Identifiers

    • 1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl-
    • 1-(3-Dipropylaminopropyl)homopiperazine
    • 1-(3-DipropylaMino-propyl)hoMopiperazine
    • 3-(1,4-diazepan-1-yl)-N,N-dipropylpropan-1-amine
    • 1-(3-dipropylamino-propyl)homopiperazine, AldrichCPR
    • 827614-53-9
    • 1-(3-dipropylaminopropyl)-homopiperazine
    • MFCD03701085
    • 1-(3-dipropylamino-propyl)-homopiperazine
    • DTXSID40374454
    • MDL: MFCD03701085
    • Inchi: 1S/C14H31N3/c1-3-9-16(10-4-2)12-6-13-17-11-5-7-15-8-14-17/h15H,3-14H2,1-2H3
    • InChI Key: MIZVQJBPSCHNND-UHFFFAOYSA-N
    • SMILES: N1(CCNCCC1)CCCN(CCC)CCC

Computed Properties

  • Exact Mass: 241.252
  • Monoisotopic Mass: 241.252
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 8
  • Complexity: 167
  • 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: 2.1
  • Topological Polar Surface Area: 18.5?2

1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl- Pricemore >>

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1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl- Related Literature

Additional information on 1H-1,4-Diazepine-1-propanamine,hexahydro-N,N-dipropyl-

Comprehensive Overview of 1H-1,4-Diazepine-1-propanamine, hexahydro-N,N-dipropyl- (CAS No. 827614-53-9)

1H-1,4-Diazepine-1-propanamine, hexahydro-N,N-dipropyl- (CAS No. 827614-53-9) is a specialized organic compound belonging to the diazepine class, which has garnered significant attention in pharmaceutical and chemical research. This compound, characterized by its unique hexahydro-N,N-dipropyl structure, is often explored for its potential applications in drug development and biochemical studies. Researchers are particularly interested in its diazepine core, which is known for its versatility in medicinal chemistry.

The molecular structure of 1H-1,4-Diazepine-1-propanamine features a seven-membered ring with two nitrogen atoms, contributing to its stability and reactivity. The hexahydro modification enhances its solubility and bioavailability, making it a candidate for further pharmacological investigations. The N,N-dipropyl side chains further modify its properties, influencing its interaction with biological targets. This compound is often discussed in the context of central nervous system (CNS) research, as diazepine derivatives are known to exhibit neurological activity.

In recent years, the demand for 1H-1,4-Diazepine-1-propanamine derivatives has increased due to their potential role in addressing neurological disorders. With the rise of neurodegenerative diseases and mental health conditions, researchers are actively exploring novel compounds that can modulate neurotransmitter systems. The hexahydro-N,N-dipropyl variant is particularly intriguing due to its balanced lipophilicity and metabolic stability, which are critical factors in drug design.

From a synthetic chemistry perspective, 827614-53-9 serves as a valuable intermediate in the preparation of more complex molecules. Its diazepine scaffold is frequently utilized in the synthesis of heterocyclic compounds, which are pivotal in developing new therapeutic agents. The compound's compatibility with various reaction conditions makes it a preferred choice for medicinal chemists and pharmaceutical researchers.

The global market for 1H-1,4-Diazepine-1-propanamine and its derivatives is expanding, driven by advancements in drug discovery technologies and increasing investment in biopharmaceutical research. Companies specializing in fine chemicals and custom synthesis are actively stocking this compound to meet the growing demand from academic and industrial laboratories. Additionally, the rise of AI-driven drug discovery has further accelerated the exploration of diazepine-based molecules, including hexahydro-N,N-dipropyl variants.

Quality control and regulatory compliance are paramount when handling CAS No. 827614-53-9. Reputable suppliers ensure that the compound is synthesized under strict guidelines to maintain purity and consistency. Analytical techniques such as HPLC, NMR, and mass spectrometry are routinely employed to verify the identity and quality of the material, ensuring it meets the standards required for research and development.

In conclusion, 1H-1,4-Diazepine-1-propanamine, hexahydro-N,N-dipropyl- (CAS No. 827614-53-9) represents a promising compound in the realm of pharmaceutical and chemical sciences. Its structural features and potential applications make it a subject of ongoing research, particularly in the fields of neurology and drug development. As scientific understanding of diazepine derivatives deepens, this compound is likely to play an increasingly significant role in the development of next-generation therapeutics.

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