Cas no 97266-25-6 (2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine)

2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine is a tertiary amine compound featuring a pyridinylmethyl substituent, offering versatile reactivity in organic synthesis. Its structure combines a sterically hindered tert-butyl group with a pyridine moiety, making it useful as a ligand or intermediate in catalytic and pharmaceutical applications. The pyridine ring enhances coordination properties, while the bulky alkyl group may influence selectivity in reactions. This compound is typically employed in the development of bioactive molecules or as a building block for complex heterocycles. Its stability and functional group compatibility make it a valuable reagent for researchers exploring nitrogen-containing frameworks. Proper handling under inert conditions is recommended due to potential sensitivity.
2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine structure
97266-25-6 structure
Product Name:2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine
CAS No:97266-25-6
MF:C10H16N2
MW:164.247442245483
MDL:MFCD00716871
CID:1085498
PubChem ID:961528
Update Time:2025-05-21

2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine Chemical and Physical Properties

Names and Identifiers

    • 2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine
    • N-(tert-butyl)-N-(pyridin-3-ylmethyl)amine
    • SCHEMBL7750983
    • MFCD00716871
    • BB 0219000
    • DTXSID90359392
    • BS-36421
    • EN300-50280
    • N-[(3-pyridyl)methyl]-(1,1-dimethylethyl)amine
    • Z56175304
    • tert-butyl(pyridin-3-ylmethyl)amine
    • QSDPAWDWCPJGAE-UHFFFAOYSA-N
    • CS-0250270
    • AKOS000133295
    • 2-METHYL-N-(3-PYRIDINYLMETHYL)-2-PROPANAMINE
    • 97266-25-6
    • tert-butyl[(pyridin-3-yl)methyl]amine
    • STK510905
    • N-(3-Pyridinylmethyl)-tert-butylamine
    • MDL: MFCD00716871
    • Inchi: 1S/C10H16N2/c1-10(2,3)12-8-9-5-4-6-11-7-9/h4-7,12H,8H2,1-3H3
    • InChI Key: QSDPAWDWCPJGAE-UHFFFAOYSA-N
    • SMILES: N(CC1C=NC=CC=1)C(C)(C)C

Computed Properties

  • Exact Mass: 164.131348519g/mol
  • Monoisotopic Mass: 164.131348519g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 3
  • Complexity: 126
  • 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: 1.4
  • Topological Polar Surface Area: 24.9?2

Experimental Properties

  • Density: 0.9±0.1 g/cm3
  • Melting Point: 162-171 °C
  • Boiling Point: 242.0±15.0 °C at 760 mmHg
  • Flash Point: 100.2±20.4 °C
  • Vapor Pressure: 0.0±0.5 mmHg at 25°C

2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine Security Information

2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine Pricemore >>

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Additional information on 2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine

2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine: A Comprehensive Overview

2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine, also known by its CAS number 97266-25-6, is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound, characterized by its unique structure and properties, has garnered attention in recent years due to its potential in drug discovery, catalysis, and advanced materials development. The molecule consists of a pyridine ring attached to a methyl-substituted amine group, which imparts it with distinctive electronic and steric properties.

Recent studies have highlighted the role of 2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine in the synthesis of bioactive compounds. Researchers have explored its ability to act as a chiral ligand in asymmetric catalysis, facilitating the production of enantiomerically enriched pharmaceutical intermediates. This application is particularly promising given the increasing demand for enantioselective processes in the pharmaceutical industry.

The synthesis of CAS 97266-25-6 involves a multi-step process that typically begins with the preparation of the pyridine derivative. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses, reducing production costs and minimizing waste. These improvements are critical for scaling up production to meet industrial demands.

In addition to its role in catalysis, 2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amine has been investigated for its potential in polymer chemistry. Its ability to form stable coordination complexes with transition metals makes it a valuable component in the development of novel polymers with tailored properties. These materials hold promise for applications in electronics, optics, and advanced composites.

The compound's electronic properties have also been leveraged in the field of electrochemistry. Studies have demonstrated its utility as an electrode material in supercapacitors and batteries, where it exhibits high energy density and excellent cycle stability. This finding underscores its potential for contributing to the development of next-generation energy storage systems.

Furthermore, recent research has explored the use of CAS 97266-25-6 as a building block for constructing supramolecular assemblies. Its ability to form hydrogen bonds and π–π interactions enables the creation of complex architectures with applications in sensing, drug delivery, and nanotechnology.

In conclusion, 2-Methyl-N-(pyridin-3-ylmethyl)propan-2-amime, with its unique structure and diverse functional groups, continues to be a focal point in modern chemical research. Its applications span across multiple disciplines, driven by advancements in synthesis techniques and an increased understanding of its properties. As research progresses, this compound is expected to play an even more significant role in shaping future innovations across various industries.

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