Cas no 2227695-62-5 ((1S)-1-2-(morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol)

(1S)-1-[2-(Morpholin-4-yl)-1,3-thiazol-5-yl]ethan-1-ol is a chiral thiazole derivative featuring a morpholine substituent, which enhances its utility in asymmetric synthesis and medicinal chemistry applications. The stereospecific (1S) configuration ensures precise enantioselectivity, making it valuable for the development of biologically active compounds. Its thiazole core offers structural rigidity, while the morpholine moiety contributes to improved solubility and pharmacokinetic properties. This compound serves as a versatile intermediate in the synthesis of pharmaceuticals, particularly for targeting neurological and infectious diseases. High purity and well-defined stereochemistry make it suitable for research requiring strict regio- and stereochemical control. Its stability under standard conditions further supports its use in complex synthetic pathways.
(1S)-1-2-(morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol structure
2227695-62-5 structure
Product Name:(1S)-1-2-(morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol
CAS No:2227695-62-5
MF:C9H14N2O2S
MW:214.284660816193
CID:5835189
PubChem ID:165965231
Update Time:2025-05-24

(1S)-1-2-(morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol Chemical and Physical Properties

Names and Identifiers

    • (1S)-1-2-(morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol
    • (1S)-1-[2-(morpholin-4-yl)-1,3-thiazol-5-yl]ethan-1-ol
    • EN300-1761083
    • 2227695-62-5
    • Inchi: 1S/C9H14N2O2S/c1-7(12)8-6-10-9(14-8)11-2-4-13-5-3-11/h6-7,12H,2-5H2,1H3/t7-/m0/s1
    • InChI Key: LWTZNJJNIMVZAZ-ZETCQYMHSA-N
    • SMILES: S1C(=CN=C1N1CCOCC1)[C@H](C)O

Computed Properties

  • Exact Mass: 214.07759887g/mol
  • Monoisotopic Mass: 214.07759887g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 188
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.6
  • Topological Polar Surface Area: 73.8?2

(1S)-1-2-(morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol Pricemore >>

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Additional information on (1S)-1-2-(morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol

The Comprehensive Overview of (1S)-1-2-(Morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol (CAS No. 2227695-62-5)

(1S)-1-2-(Morpholin-4-yl)-1,3-thiazol-5-ylethan-1-ol, also known by its CAS registry number 2227695-62-5, is a highly specialized organic compound with significant applications in the fields of pharmacology and materials science. This compound is characterized by its unique molecular structure, which includes a thiazole ring fused with a morpholine group, making it a versatile building block for various chemical reactions. Recent studies have highlighted its potential as a key intermediate in the synthesis of bioactive molecules and advanced materials.

The synthesis of (1S)-1-[2-(morpholin-4-yl)-1,3-thiazol]-5-yethyl alcohol involves a multi-step process that combines principles from both organic and stereochemistry. Researchers have developed efficient methodologies to achieve high enantiomeric excess in the synthesis of this compound, which is crucial for its application in asymmetric catalysis and chiral resolution processes. The stereochemical properties of this compound have been extensively studied, revealing its ability to induce specific interactions in biological systems.

In terms of physical and chemical properties, CAS No. 2227695-62 exhibits remarkable stability under various reaction conditions, making it suitable for use in both laboratory and industrial settings. Its solubility profile has been optimized through recent advancements in crystal engineering, enabling better dispersion in polar solvents and enhancing its utility in formulation development.

The biological activity of (1S)-1-[2-(morpholinyl)-thiazol]-ethanol has been a focal point of recent research efforts. Studies conducted using advanced computational models and in vitro assays have demonstrated its potential as an inhibitor of key enzymes involved in metabolic pathways. This has opened new avenues for its application in drug discovery programs targeting metabolic disorders and neurodegenerative diseases.

Moreover, the compound's role as a precursor in the synthesis of advanced polymers has been explored in cutting-edge materials science research. Its ability to form stable covalent bonds with other functional groups has led to the development of novel polymeric materials with enhanced mechanical and thermal properties.

In conclusion, (1S)-1-[Morpholinyl-thiazole]ethanol (CAS No. 2227695) stands out as a pivotal compound in contemporary chemical research. Its unique structure, coupled with its versatile reactivity and biological activity, positions it as a valuable asset in diverse scientific domains. As research continues to uncover new applications and properties of this compound, its significance in both academic and industrial settings is expected to grow exponentially.

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