Cas no 2206243-38-9 (2-(2-methylpropyl)morpholine hydrochloride)

2-(2-Methylpropyl)morpholine hydrochloride is a morpholine derivative with a branched alkyl substituent, offering utility as an intermediate in organic synthesis and pharmaceutical applications. Its hydrochloride salt form enhances stability and solubility, facilitating handling and reactivity in various chemical processes. The compound’s structural features, including the morpholine ring and isobutyl group, contribute to its versatility in forming derivatives or acting as a building block for bioactive molecules. Its well-defined chemical properties make it suitable for controlled reactions in medicinal chemistry and material science. The product is typically characterized by high purity, ensuring consistency in research and industrial applications.
2-(2-methylpropyl)morpholine hydrochloride structure
2206243-38-9 structure
Product Name:2-(2-methylpropyl)morpholine hydrochloride
CAS No:2206243-38-9
MF:C8H18ClNO
MW:179.687621593475
MDL:MFCD30726128
CID:5462005
PubChem ID:77349666
Update Time:2025-10-28

2-(2-methylpropyl)morpholine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-Isobutylmorpholine hydrochloride
    • 2-(2-methylpropyl)morpholine;hydrochloride
    • starbld0046365
    • EN300-23609869
    • Z4628240194
    • 2206243-38-9
    • 2-(2-methylpropyl)morpholine hydrochloride
    • MDL: MFCD30726128
    • Inchi: 1S/C8H17NO.ClH/c1-7(2)5-8-6-9-3-4-10-8;/h7-9H,3-6H2,1-2H3;1H
    • InChI Key: ULDJYUOLUOAZHY-UHFFFAOYSA-N
    • SMILES: Cl.O1CCNCC1CC(C)C

Computed Properties

  • Exact Mass: 179.1076919g/mol
  • Monoisotopic Mass: 179.1076919g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 93.3
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 21.3?2

2-(2-methylpropyl)morpholine hydrochloride Pricemore >>

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Additional information on 2-(2-methylpropyl)morpholine hydrochloride

2-(2-Methylpropyl)Morpholine Hydrochloride: A Comprehensive Overview

The compound with CAS No. 2206243-38-9, commonly referred to as 2-(2-methylpropyl)morpholine hydrochloride, is a significant entity in the field of organic chemistry and pharmacology. This compound has garnered attention due to its unique chemical structure and potential applications in various industries, particularly in the pharmaceutical sector. In this article, we will delve into the properties, synthesis, and recent advancements related to 2-(2-methylpropyl)morpholine hydrochloride, providing a detailed and up-to-date analysis.

The chemical structure of 2-(2-methylpropyl)morpholine hydrochloride consists of a morpholine ring, which is a six-membered ring containing one oxygen atom and one nitrogen atom. The morpholine ring is substituted at the 2-position with a 2-methylpropyl group, also known as an isobutyl group. This substitution imparts unique electronic and steric properties to the molecule, making it versatile for various chemical reactions and biological applications. The hydrochloride salt form indicates that the compound exists as a chloride ion pair, which is often preferred for its stability and solubility in aqueous solutions.

Recent studies have highlighted the potential of 2-(2-methylpropyl)morpholine hydrochloride as a precursor in the synthesis of bioactive compounds. For instance, researchers have explored its role in the development of novel antiviral agents and anticancer drugs. The morpholine moiety is known for its ability to form hydrogen bonds, which is crucial for drug-target interactions. The presence of the isobutyl group further enhances the molecule's lipophilicity, enabling better penetration into biological membranes.

In terms of synthesis, 2-(2-methylpropyl)morpholine hydrochloride can be prepared through various routes, including nucleophilic substitution and ring-opening reactions. One common method involves the reaction of morpholine with an appropriate alkylating agent, such as 1-bromo-2-methylpropane, followed by acidification to obtain the hydrochloride salt. Optimization of reaction conditions, such as temperature and solvent choice, has been shown to significantly influence the yield and purity of the final product.

The pharmacological properties of in-depth studies on 2-(2-methylpropyl)morpholine hydrochloride have revealed its potential as a building block in drug discovery. For example, it has been used in the synthesis of inhibitors for various enzymes, including kinases and proteases. These enzymes are often implicated in diseases such as cancer, inflammation, and viral infections. By modifying the substituents on the morpholine ring or altering the length of the alkyl chain, researchers can fine-tune the compound's activity and selectivity.

Beyond its pharmaceutical applications, the use cases of 2-(2-methylpropyl)morpholine hydrochloride extend to other areas such as agrochemicals and materials science. In agrochemistry, derivatives of this compound have been investigated for their pesticidal activity against various plant pathogens. Its ability to form stable complexes with metal ions also makes it a promising candidate for coordination chemistry studies.

In conclusion, CAS No. 2206243-38-9: 2-(Methylpropyl)Morpholine Hydrochloride stands out as a versatile compound with diverse applications across multiple disciplines. Its unique chemical structure and favorable physicochemical properties make it an invaluable tool in both academic research and industrial development. As ongoing research continues to uncover new avenues for its utilization, this compound is poised to play an increasingly important role in advancing scientific knowledge and therapeutic interventions.

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