Cas no 91253-14-4 (N4-[2-(morpholin-4-yl)ethyl]pyridine-3,4-diamine)

N4-[2-(morpholin-4-yl)ethyl]pyridine-3,4-diamine is a heterocyclic organic compound featuring both pyridine and morpholine moieties, offering versatile reactivity for pharmaceutical and chemical synthesis applications. Its bifunctional structure, combining an aromatic amine and a morpholine-substituted ethyl linker, makes it a valuable intermediate in the development of bioactive molecules, particularly in kinase inhibitor research. The compound’s electron-rich pyridine core and secondary amine group facilitate selective modifications, while the morpholine component enhances solubility and pharmacokinetic properties. Its well-defined synthetic route ensures high purity and consistency, making it suitable for rigorous research in medicinal chemistry and drug discovery.
N4-[2-(morpholin-4-yl)ethyl]pyridine-3,4-diamine structure
91253-14-4 structure
Product Name:N4-[2-(morpholin-4-yl)ethyl]pyridine-3,4-diamine
CAS No:91253-14-4
MF:C11H18N4O
MW:222.286821842194
CID:2190732
PubChem ID:14174124
Update Time:2025-06-08

N4-[2-(morpholin-4-yl)ethyl]pyridine-3,4-diamine Chemical and Physical Properties

Names and Identifiers

    • N4-[2-(4-morpholinyl)ethyl]-3,4-pyridinediamine
    • N4-(2-Morpholinoethyl)pyridine-3,4-diamine
    • OR302728
    • AK161191
    • BC4170493
    • AX8294151
    • ST24048760
    • 4-N-(2-morpholin-4-ylethyl)pyridine-3,4-diamine
    • N4-[2-(morpholin-4-yl)ethyl]pyridine-3,4-diamine
    • Inchi: 1S/C11H18N4O/c12-10-9-13-2-1-11(10)14-3-4-15-5-7-16-8-6-15/h1-2,9H,3-8,12H2,(H,13,14)
    • InChI Key: MJRBSCNJGKZPSX-UHFFFAOYSA-N
    • SMILES: O1CCN(CCNC2C=CN=CC=2N)CC1

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 4
  • Complexity: 196
  • Topological Polar Surface Area: 63.4

N4-[2-(morpholin-4-yl)ethyl]pyridine-3,4-diamine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Chemenu
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Enamine
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Enamine
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Enamine
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Enamine
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