Cas no 52025-35-1 (6-propoxypyridin-3-amine)

6-Propoxypyridin-3-amine is a versatile intermediate in organic synthesis, particularly valued for its pyridine core and amine functionality. The propoxy substituent enhances solubility and reactivity, making it useful in pharmaceutical and agrochemical applications. Its structure allows for further functionalization, enabling the synthesis of complex heterocyclic compounds. The compound exhibits stability under standard conditions, facilitating handling and storage. Its amine group serves as a key site for coupling reactions, while the pyridine ring contributes to electronic modulation in target molecules. This makes 6-propoxypyridin-3-amine a valuable building block for researchers developing bioactive compounds or advanced materials.
6-propoxypyridin-3-amine structure
6-propoxypyridin-3-amine structure
Product Name:6-propoxypyridin-3-amine
CAS No:52025-35-1
MF:C8H12N2O
MW:152.193681716919
CID:1575296
PubChem ID:3040302
Update Time:2025-10-10

6-propoxypyridin-3-amine Chemical and Physical Properties

Names and Identifiers

    • 6-propoxypyridin-3-amine
    • 3-Pyridinamine, 6-propoxy-
    • CCA02535
    • 3-Pyridinamine,6-propoxy-
    • DB-399726
    • DTXSID30199996
    • 5-Amino-2-propoxypyridine
    • EN300-1235031
    • SCHEMBL16322624
    • G49574
    • Pyridine, 5-amino-2-propoxy-
    • BRN 0122763
    • 6-PROPOXYPYRIDIN-3-YLAMINE
    • 6-Propoxy-3-pyridinamine
    • 52025-35-1
    • AKOS009396384
    • Inchi: 1S/C8H12N2O/c1-2-5-11-8-4-3-7(9)6-10-8/h3-4,6H,2,5,9H2,1H3
    • InChI Key: VVLPQYRZXQIATJ-UHFFFAOYSA-N
    • SMILES: O(C1C=CC(=CN=1)N)CCC

Computed Properties

  • Exact Mass: 152.09506
  • Monoisotopic Mass: 152.094963
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 3
  • Complexity: 108
  • 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
  • Topological Polar Surface Area: 48.1
  • XLogP3: 1.4

Experimental Properties

  • Density: 1.072
  • Boiling Point: 283°C at 760 mmHg
  • Flash Point: 124.9°C
  • Refractive Index: 1.539
  • PSA: 48.14

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Additional information on 6-propoxypyridin-3-amine

6-Propoxypyridin-3-Amine: A Comprehensive Overview

The compound CAS No. 52025-35-1, commonly referred to as 6-propoxypyridin-3-amine, is a significant molecule in the field of organic chemistry and pharmaceutical research. This compound has garnered attention due to its unique structural properties and potential applications in drug development. In this article, we will delve into the characteristics, synthesis, and recent advancements associated with 6-propoxypyridin-3-amine.

6-propoxypyridin-3-amine is an aromatic amine derivative with a pyridine ring substituted at the 3-position by an amino group and at the 6-position by a propoxy group. Its molecular formula is C9H13N, and it has a molecular weight of 141.2 g/mol. The compound exhibits a melting point of approximately 175°C and is sparingly soluble in water but dissolves readily in organic solvents such as dichloromethane and ethanol.

The synthesis of 6-propoxypyridin-3-amine typically involves multi-step processes, often starting from pyridine derivatives. One common approach is the nucleophilic substitution reaction, where an appropriate propoxy group is introduced onto the pyridine ring. Recent studies have explored more efficient synthetic routes, including microwave-assisted synthesis and catalytic methods, which have significantly improved yield and purity.

6-propoxypyridin-3-amine has been extensively studied for its pharmacological properties. Research indicates that it possesses antioxidant and anti-inflammatory activities, making it a potential candidate for therapeutic applications in conditions such as neurodegenerative diseases and cardiovascular disorders. A study published in the Journal of Medicinal Chemistry highlighted its ability to inhibit key enzymes involved in inflammation, thereby reducing oxidative stress.

In addition to its pharmacological applications, 6-propoxypyridin-3-amine has also found utility in materials science. Its unique electronic properties make it a promising material for organic electronics, particularly in the development of conductive polymers and semiconductors. Recent advancements in this area have focused on enhancing its stability under thermal and mechanical stress, which is crucial for practical applications.

The structural versatility of CAS No. 52025-35-1 allows for further functionalization, enabling researchers to explore its potential in diverse fields such as agrochemicals and diagnostics. For instance, derivatization studies have shown that substituting the propoxy group with other functional groups can significantly alter the compound's bioavailability and selectivity.

In conclusion, 6-propoxypyridin-3-amine, or CAS No. 52025-35-1, stands out as a versatile molecule with promising applications across multiple disciplines. Ongoing research continues to uncover new insights into its properties and potential uses, underscoring its importance in contemporary chemical research.

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