Cas no 39630-25-6 (2-(piperidin-1-ylcarbonyl)phenylamine)

2-(piperidin-1-ylcarbonyl)phenylamine structure
39630-25-6 structure
Product Name:2-(piperidin-1-ylcarbonyl)phenylamine
CAS No:39630-25-6
MF:C12H16N2O
MW:204.268242835999
MDL:MFCD00448737
CID:316546
PubChem ID:558730
Update Time:2025-10-29

2-(piperidin-1-ylcarbonyl)phenylamine Chemical and Physical Properties

Names and Identifiers

    • Methanone,(2-aminophenyl)-1-piperidinyl-
    • (2-aminophenyl)-1-piperidinylMethanone
    • [2-(Piperidin-1-ylcarbonyl)phenyl]amine
    • 2-(Piperidin-1-ylcarbonyl)aniline
    • (2-aminophenyl)(piperidin-1-yl)methanone
    • [2-(1-piperidinylcarbonyl)phenyl]amine
    • 1-(2-aminobenzoyl)piperidine
    • 1-(2-amino-benzoyl)-piperidine
    • 1-anthraniloyl-piperidine
    • 2-(1-Piperidinylcarbonyl)aniline
    • 2-(piperidin-1-yl-carbonyl)-aniline
    • 2-(piperidine-1-carbonyl)aniline
    • 2-aminophenyl piperidyl ketone
    • AC1LBIVH
    • ST027943
    • DTXSID20339788
    • Oprea1_206998
    • SR-01000318946-1
    • 2-(5-Chloro-2H-benzotriazol-2-yl)-6-(1,1-dimethylethyl)-4-ethenylphenol
    • (2-aminophenyl)-(1-piperidyl)methanone
    • SR-01000318946
    • Piperidine, 1-(2-aminobenzoyl)-
    • FT-0677469
    • Z56040655
    • BB 0220216
    • CS-0307882
    • SCHEMBL2302867
    • A873604
    • (2-Aminophenyl)-piperidin-1-yl-methanone
    • (2-aminophenyl)(1-piperidyl)methanone
    • AKOS000111585
    • 39630-25-6
    • EN300-09702
    • (2-aminophenyl)-piperidin-1-ylmethanone
    • 2-(1-Piperidinylcarbonyl)aniline #
    • MFCD00448737
    • BAS 00884076
    • 2-(piperidin-1-ylcarbonyl)phenylamine
    • MDL: MFCD00448737
    • Inchi: 1S/C12H16N2O/c13-11-7-3-2-6-10(11)12(15)14-8-4-1-5-9-14/h2-3,6-7H,1,4-5,8-9,13H2
    • InChI Key: YJTQPHOSNYIGPC-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC=CC=1N)N1CCCCC1

Computed Properties

  • Exact Mass: 204.12638
  • Monoisotopic Mass: 204.126263138g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 2
  • Complexity: 224
  • 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: 46.3?2

Experimental Properties

  • Density: 1.1±0.1 g/cm3
  • Boiling Point: 218.9±13.0 °C at 760 mmHg
  • Flash Point: 86.2±19.8 °C
  • PSA: 46.33
  • Vapor Pressure: 0.1±0.4 mmHg at 25°C

2-(piperidin-1-ylcarbonyl)phenylamine Security Information

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2-(piperidin-1-ylcarbonyl)phenylamine Related Literature

Additional information on 2-(piperidin-1-ylcarbonyl)phenylamine

2-(Piperidin-1-ylcarbonyl)phenylamine (CAS No. 39630-25-6): A Comprehensive Overview

2-(Piperidin-1-ylcarbonyl)phenylamine (CAS No. 39630-25-6) is a specialized organic compound that has garnered significant attention in pharmaceutical and chemical research. This compound, also known as N-(2-aminophenyl)-1-piperidinecarboxamide, features a unique molecular structure combining a phenylamine group with a piperidine carbonyl moiety. Its versatility in synthesis and potential applications make it a subject of interest for researchers and industry professionals alike.

The molecular formula of 2-(piperidin-1-ylcarbonyl)phenylamine is C12H16N2O, with a molecular weight of 204.27 g/mol. The compound exhibits moderate solubility in organic solvents such as dimethyl sulfoxide (DMSO) and methanol, while being less soluble in water. Its melting point ranges between 120-125°C, and it typically appears as a white to off-white crystalline powder under standard conditions.

In recent years, 2-(piperidin-1-ylcarbonyl)phenylamine has emerged as a valuable intermediate in medicinal chemistry. Researchers have explored its potential as a building block for various pharmaceutical compounds, particularly in the development of central nervous system (CNS) drugs. The piperidine moiety, a common feature in many bioactive molecules, contributes to the compound's ability to interact with biological targets, while the phenylamine group offers opportunities for further chemical modifications.

The synthesis of 2-(piperidin-1-ylcarbonyl)phenylamine typically involves the reaction between 2-aminobenzoic acid derivatives and piperidine in the presence of coupling reagents. Recent advancements in green chemistry approaches have focused on optimizing this synthesis to reduce environmental impact while maintaining high yields. These developments align with current industry trends toward sustainable chemical production, a topic of growing importance in scientific communities and among environmentally conscious consumers.

Analytical characterization of 39630-25-6 commonly employs techniques such as nuclear magnetic resonance (NMR) spectroscopy, high-performance liquid chromatography (HPLC), and mass spectrometry. These methods ensure the compound's purity and confirm its structural integrity, which is crucial for research and industrial applications. Quality control measures for 2-(piperidin-1-ylcarbonyl)phenylamine typically specify a minimum purity of 98%, with strict limits on residual solvents and impurities.

The pharmaceutical industry has shown particular interest in 2-(piperidin-1-ylcarbonyl)phenylamine derivatives due to their potential biological activities. Recent studies suggest that modifications of this core structure may lead to compounds with interesting pharmacological properties, though extensive research is still ongoing. This aligns with current search trends where users frequently inquire about "new drug intermediates" and "potential CNS drug candidates."

From a commercial perspective, the market for 39630-25-6 has seen steady growth, particularly in regions with strong pharmaceutical manufacturing sectors. Suppliers typically offer this compound in quantities ranging from milligrams to kilograms, catering to both research laboratories and industrial-scale operations. The global demand for specialized chemical intermediates continues to rise, driven by increased investment in drug discovery and development.

Storage and handling recommendations for 2-(piperidin-1-ylcarbonyl)phenylamine suggest keeping the compound in a cool, dry environment, protected from light and moisture. While not classified as hazardous under standard regulations, proper laboratory practices should be followed when working with this material. These precautions reflect current industry standards for chemical safety, a topic frequently searched by professionals in the field.

Recent scientific literature highlights several innovative applications of 2-(piperidin-1-ylcarbonyl)phenylamine in materials science beyond its pharmaceutical uses. Researchers have explored its potential as a component in advanced materials and as a ligand in catalytic systems. These developments correspond to growing interest in "multifunctional chemical building blocks" among researchers and industry professionals searching for novel applications of existing compounds.

The future outlook for 39630-25-6 appears promising, with ongoing research exploring new synthetic routes and potential applications. As the chemical industry continues to evolve toward more specialized and efficient production methods, compounds like 2-(piperidin-1-ylcarbonyl)phenylamine are likely to maintain their relevance in both academic and industrial settings. This aligns with current search trends focusing on "emerging chemical intermediates" and "future of specialty chemicals."

For researchers considering working with 2-(piperidin-1-ylcarbonyl)phenylamine, it's important to consult recent literature and safety data sheets. The compound's versatility makes it suitable for various experimental designs, particularly in medicinal chemistry and materials science. As with any chemical substance, proper characterization and purity verification are essential before use in sensitive applications.

In conclusion, 2-(piperidin-1-ylcarbonyl)phenylamine (CAS No. 39630-25-6) represents an interesting case study in the intersection of chemical synthesis and applied research. Its balanced properties as a chemical intermediate, combined with potential pharmaceutical applications, ensure its continued importance in scientific research and industrial chemistry. The compound's story reflects broader trends in chemical innovation, where traditional molecules find new life through creative applications and modern synthetic approaches.

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