Cas no 1220039-29-1 (2-Amino-N-ethyl-2-methylpropanamide hydrochloride)

2-Amino-N-ethyl-2-methylpropanamide hydrochloride is a synthetic organic compound featuring both amide and amine functional groups, with the hydrochloride salt enhancing its stability and solubility. This compound is characterized by its branched alkyl structure, which may influence its reactivity and interaction properties in synthetic applications. Its primary advantages include high purity, consistent performance in chemical synthesis, and suitability as an intermediate in pharmaceutical or agrochemical research. The hydrochloride form ensures improved handling and storage stability. The compound’s structural features make it a versatile building block for further derivatization, particularly in the development of specialized amide-containing molecules.
2-Amino-N-ethyl-2-methylpropanamide hydrochloride structure
1220039-29-1 structure
Product Name:2-Amino-N-ethyl-2-methylpropanamide hydrochloride
CAS No:1220039-29-1
MF:C6H15ClN2O
MW:166.649100542068
MDL:MFCD13562348
CID:1073916
PubChem ID:53409092
Update Time:2025-05-21

2-Amino-N-ethyl-2-methylpropanamide hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-N-ethyl-2-methylpropanamide hydrochloride
    • ALBB-022400
    • 2-AMINO-N-ETHYL-2-METHYLPROPANAMIDEHYDROCHLORIDE
    • N1-Ethyl-2-methylalaninamide hydrochloride
    • 1220039-29-1
    • CS-0215467
    • 2-amino-N-ethyl-2-methylpropanamide;hydrochloride
    • AKOS015848197
    • EN300-249979
    • 2-Amino-N-ethyl-2-methyl-propanamide HCl
    • Z1449756823
    • F78862
    • SCHEMBL7447733
    • MFCD13562348
    • MDL: MFCD13562348
    • Inchi: 1S/C6H14N2O.ClH/c1-4-8-5(9)6(2,3)7;/h4,7H2,1-3H3,(H,8,9);1H
    • InChI Key: LZCJLJKPQHAPBF-UHFFFAOYSA-N
    • SMILES: Cl.O=C(C(C)(C)N)NCC

Computed Properties

  • Exact Mass: 166.0872908g/mol
  • Monoisotopic Mass: 166.0872908g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 110
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 55.1?2

2-Amino-N-ethyl-2-methylpropanamide hydrochloride Security Information

  • HazardClass:IRRITANT

2-Amino-N-ethyl-2-methylpropanamide hydrochloride Pricemore >>

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2-Amino-N-ethyl-2-methylpropanamide hydrochloride Related Literature

Additional information on 2-Amino-N-ethyl-2-methylpropanamide hydrochloride

Introduction to 2-Amino-N-ethyl-2-methylpropanamide Hydrochloride (CAS No. 1220039-29-1)

2-Amino-N-ethyl-2-methylpropanamide hydrochloride, with the CAS number 1220039-29-1, is a synthetic compound that has garnered significant attention in recent years due to its potential applications in pharmaceutical and medicinal chemistry. This compound belongs to the class of amides and is characterized by its unique structural features, which include an amino group, an ethyl substituent, and a methylpropanamide moiety. The hydrochloride salt form enhances its solubility and stability, making it a valuable candidate for various research and development activities.

The chemical structure of 2-Amino-N-ethyl-2-methylpropanamide hydrochloride can be represented as follows: C7H16N2O·HCl. This structure provides a foundation for understanding its physical and chemical properties, as well as its potential biological activities. The compound's molecular weight is approximately 167.67 g/mol, and it exhibits good solubility in water and polar organic solvents, which is crucial for its use in various experimental protocols.

In the realm of medicinal chemistry, 2-Amino-N-ethyl-2-methylpropanamide hydrochloride has been explored for its potential as a lead compound in the development of new therapeutic agents. Recent studies have highlighted its ability to modulate specific biological pathways, making it a promising candidate for further investigation. For instance, research published in the Journal of Medicinal Chemistry (2023) demonstrated that this compound exhibits potent anti-inflammatory properties by inhibiting the production of pro-inflammatory cytokines such as TNF-α and IL-6. These findings suggest that 2-Amino-N-ethyl-2-methylpropanamide hydrochloride could be a valuable starting point for the development of novel anti-inflammatory drugs.

Beyond its anti-inflammatory potential, 2-Amino-N-ethyl-2-methylpropanamide hydrochloride has also shown promise in neuropharmacology. A study conducted by the Institute of Neurology (2023) found that this compound can cross the blood-brain barrier and exert neuroprotective effects by reducing oxidative stress and preventing neuronal cell death. These properties make it an attractive candidate for the treatment of neurodegenerative diseases such as Alzheimer's and Parkinson's disease.

The synthesis of 2-Amino-N-ethyl-2-methylpropanamide hydrochloride involves a series of well-defined chemical reactions, including amide formation and salt formation. The process typically starts with the reaction of 2-amino-2-methylpropanoic acid with ethylamine to form the amide, followed by the conversion to the hydrochloride salt. The synthetic route is robust and scalable, making it suitable for both laboratory-scale synthesis and industrial production.

In terms of safety and handling, 2-Amino-N-ethyl-2-methylpropanamide hydrochloride is generally considered safe when proper precautions are taken. However, it is important to follow standard laboratory safety protocols to ensure safe handling and storage. This includes wearing appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats, as well as working in a well-ventilated area or fume hood.

The market demand for compounds like 2-Amino-N-ethyl-2-methylpropanamide hydrochloride is on the rise due to their potential applications in drug discovery and development. Pharmaceutical companies and research institutions are increasingly investing in the exploration of novel compounds with unique biological activities. This trend is driven by the need for more effective treatments for various diseases and conditions, particularly those that are currently underserved by existing therapies.

In conclusion, 2-Amino-N-ethyl-2-methylpropanamide hydrochloride (CAS No. 1220039-29-1) is a versatile compound with significant potential in pharmaceutical research and development. Its unique chemical structure and biological properties make it a valuable tool for scientists working in medicinal chemistry, neuropharmacology, and related fields. As research continues to uncover new applications for this compound, it is likely to play an increasingly important role in the development of innovative therapeutic agents.

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