Cas no 2637-31-2 (3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine)

3-(1,2,3,4-Tetrahydroquinolin-1-yl)propan-1-amine is a nitrogen-containing heterocyclic compound featuring a tetrahydroquinoline core linked to a propylamine moiety. This structure imparts versatility in synthetic applications, particularly as an intermediate in pharmaceuticals and agrochemicals. The presence of both secondary and primary amine functionalities enhances its reactivity, enabling use in reductive amination, cyclization, and other transformations. Its rigid tetrahydroquinoline scaffold contributes to stereochemical stability, making it valuable for designing bioactive molecules. The compound is typically handled under inert conditions due to amine sensitivity. Suitable for research and industrial use, it offers a balance of reactivity and structural diversity for advanced chemical synthesis.
3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine structure
2637-31-2 structure
Product Name:3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine
CAS No:2637-31-2
MF:C12H18N2
MW:190.284722805023
CID:239917
PubChem ID:5156873
Update Time:2025-10-28

3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine Chemical and Physical Properties

Names and Identifiers

    • 3-(3,4-Dihydroquinolin-1(2H)-yl)propan-1-amine
    • 1(2H)-Quinolinepropanamine,3,4-dihydro-
    • 3-(3,4-Dihydro-2H-quinolin-1-yl)-propylamine
    • 3-(3,4-dihydroquinolin-1(2H)-yl)propan-1-amine(SALTDATA: FREE)
    • 3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine
    • LS-02632
    • 3-(3,4-dihydro-2H-quinolin-1-yl)propan-1-amine
    • HMS1704A10
    • 3-(3, 4-dihydro-2H-quinolin-1-yl)propan-1-amine
    • SCHEMBL18263330
    • 3-(3,4-Dihydro-1(2H)-quinolinyl)-1-propanamine
    • MFCD00778682
    • AKOS000137061
    • D86960
    • 2637-31-2
    • F2187-2282
    • BB 0254663
    • DTXSID20408988
    • 1(2H)-Quinolinepropanamine, 3,4-dihydro-
    • STK500339
    • ALBB-007183
    • MDL: MFCD00778682
    • Inchi: 1S/C12H18N2/c13-8-4-10-14-9-3-6-11-5-1-2-7-12(11)14/h1-2,5,7H,3-4,6,8-10,13H2
    • InChI Key: BHHICRFDCVVASL-UHFFFAOYSA-N
    • SMILES: N1(CCCN)C2C=CC=CC=2CCC1

Computed Properties

  • Exact Mass: 190.14714
  • Monoisotopic Mass: 190.146998583g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 170
  • 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: 1.9
  • Topological Polar Surface Area: 29.3?2

Experimental Properties

  • Density: 1.028
  • Boiling Point: 334.4°C at 760 mmHg
  • Flash Point: 138.1°C
  • Refractive Index: 1.555
  • PSA: 29.26

3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine Pricemore >>

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Additional information on 3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine

Chemical Compound CAS No. 2637-31-2: 3-(1,2,3,4-Tetrahydroquinolin-1-yl)Propan-1-Amine

The compound with CAS No. 2637-31-2, commonly referred to as 3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine, is a significant molecule in the field of organic chemistry. This compound belongs to the class of amines and features a unique structure that combines a tetrahydroquinoline ring system with a propylamine group. The tetrahydroquinoline moiety is a partially saturated bicyclic structure that contributes to the compound's versatility and reactivity.

Recent studies have highlighted the potential of this compound in various applications, particularly in drug discovery and material science. The tetrahydroquinoline group is known for its ability to act as a chiral auxiliary in asymmetric synthesis, making it a valuable component in the construction of complex molecules. Additionally, the amine functionality provides sites for further functionalization, enabling the synthesis of derivatives with diverse biological activities.

One of the most notable advancements involving this compound is its role in the development of novel catalysts for enantioselective reactions. Researchers have demonstrated that derivatives of 3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine can serve as effective ligands in transition metal-catalyzed processes. These ligands enhance the enantioselectivity of reactions, which is crucial in the production of chiral pharmaceuticals and agrochemicals.

In terms of physical properties, this compound exhibits a melting point of approximately 85°C and is soluble in common organic solvents such as dichloromethane and ethanol. Its solubility profile makes it suitable for use in various synthetic protocols that require precise control over reaction conditions. The compound's stability under standard storage conditions further adds to its utility in laboratory settings.

The synthesis of 3-(1,2,3,4-tetrahydroquinolin-1-yl)propan-1-amine typically involves multi-step processes that include both nucleophilic aromatic substitution and reduction reactions. Recent optimizations have focused on improving the yield and purity of the product by employing more efficient catalysts and reaction conditions. For instance, the use of microwave-assisted synthesis has been shown to significantly reduce reaction times while maintaining high product quality.

Beyond its role in catalysis and drug discovery, this compound has also found applications in materials science. Its ability to coordinate with metal ions makes it a promising candidate for use in metallopolymers and hybrid materials. Researchers are actively exploring its potential in creating advanced materials with tailored electronic and mechanical properties.

In conclusion, CAS No. 2637-31-2, or 3-(1,2,3,4-tetrahydroquinolin-1-yL)propan-amine, stands out as a versatile and valuable molecule with wide-ranging applications across multiple disciplines. Its unique structure and functional groups make it an ideal building block for constructing complex molecules and advanced materials. As research continues to uncover new possibilities for this compound, its significance in both academic and industrial settings is expected to grow further.

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