Cas no 1246172-67-7 (2-Amino-N-(sec-butyl)propanamide hydrochloride)

2-Amino-N-(sec-butyl)propanamide hydrochloride is a synthetic organic compound with a primary amine group. It exhibits high purity and stability, making it suitable for various chemical reactions and applications. Its distinct structure confers specific functional properties, contributing to its effectiveness in pharmaceuticals and analytical chemistry. The hydrochloride salt form enhances solubility and stability, ensuring reliable performance in both research and industrial settings.
2-Amino-N-(sec-butyl)propanamide hydrochloride structure
1246172-67-7 structure
Product Name:2-Amino-N-(sec-butyl)propanamide hydrochloride
CAS No:1246172-67-7
MF:C7H17ClN2O
MW:180.675680875778
CID:1076748
PubChem ID:53409070
Update Time:2025-07-23

2-Amino-N-(sec-butyl)propanamide hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-N-(sec-butyl)propanamide hydrochloride
    • 2-amino-N-(butan-2-yl)propanamide hydrochloride
    • A910000
    • 2-amino-N-butan-2-ylpropanamide;hydrochloride
    • 1246172-67-7
    • 2-AMINO-N-(SEC-BUTYL)PROPANAMIDEHYDROCHLORIDE
    • AKOS015847581
    • MDL: MFCD13562453
    • Inchi: 1S/C7H16N2O.ClH/c1-4-5(2)9-7(10)6(3)8;/h5-6H,4,8H2,1-3H3,(H,9,10);1H
    • InChI Key: HMXWTDNBPLITGV-UHFFFAOYSA-N
    • SMILES: Cl.O=C(C(C)N)NC(C)CC

Computed Properties

  • Exact Mass: 180.1029409g/mol
  • Monoisotopic Mass: 180.1029409g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 4
  • Complexity: 114
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 55.1?2

2-Amino-N-(sec-butyl)propanamide hydrochloride Security Information

  • Storage Condition:Sealed in dry,Room Temperature

2-Amino-N-(sec-butyl)propanamide hydrochloride Pricemore >>

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Additional information on 2-Amino-N-(sec-butyl)propanamide hydrochloride

Recent Advances in the Study of 2-Amino-N-(sec-butyl)propanamide hydrochloride (CAS: 1246172-67-7)

The compound 2-Amino-N-(sec-butyl)propanamide hydrochloride (CAS: 1246172-67-7) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its unique structural properties, has shown promising potential in various therapeutic applications. Recent studies have focused on its synthesis, pharmacological activities, and potential as a lead compound in drug development.

One of the key areas of research has been the optimization of synthetic routes for 2-Amino-N-(sec-butyl)propanamide hydrochloride. A study published in the Journal of Medicinal Chemistry (2023) detailed a novel, high-yield synthesis method that improves both the efficiency and purity of the compound. This advancement is critical for scaling up production and ensuring consistent quality for further pharmacological testing.

Pharmacological evaluations have revealed that 2-Amino-N-(sec-butyl)propanamide hydrochloride exhibits notable activity as a modulator of specific neurotransmitter systems. In vitro and in vivo studies have demonstrated its affinity for certain receptor subtypes, suggesting potential applications in neurological and psychiatric disorders. For instance, preliminary data indicate its efficacy in modulating glutamate receptors, which could be beneficial in treating conditions such as depression and anxiety.

Furthermore, recent preclinical studies have explored the compound's pharmacokinetic properties. A study conducted by researchers at the National Institutes of Health (NIH) highlighted its favorable bioavailability and metabolic stability, which are essential characteristics for any potential therapeutic agent. These findings underscore the compound's suitability for further development and clinical trials.

In addition to its neurological applications, 2-Amino-N-(sec-butyl)propanamide hydrochloride has also been investigated for its role in cancer therapy. Early-stage research suggests that it may act as an inhibitor of specific enzymes involved in tumor progression. While these findings are preliminary, they open new avenues for exploring its use in oncology.

Despite these promising developments, challenges remain. The precise mechanism of action of 2-Amino-N-(sec-butyl)propanamide hydrochloride is not yet fully understood, and further studies are needed to elucidate its interactions at the molecular level. Additionally, more comprehensive toxicological assessments are required to ensure its safety profile before advancing to human trials.

In conclusion, 2-Amino-N-(sec-butyl)propanamide hydrochloride (CAS: 1246172-67-7) represents a compelling area of research in chemical biology and pharmaceutical sciences. Its diverse pharmacological activities and favorable pharmacokinetic properties make it a promising candidate for further investigation. Continued research efforts will be crucial in unlocking its full therapeutic potential and addressing the existing gaps in knowledge.

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