Cas no 1480448-22-3 (2-(ethylsulfanyl)spiro3.3heptane-2-carboxylic acid)

2-(Ethylsulfanyl)spiro[3.3]heptane-2-carboxylic acid is a spirocyclic carboxylic acid derivative featuring an ethylsulfanyl substituent, which enhances its utility in synthetic and medicinal chemistry. The spiro[3.3]heptane core imparts structural rigidity, potentially improving binding selectivity in drug design. The carboxylic acid group allows for further functionalization, making it a versatile intermediate for derivatization or conjugation. Its unique scaffold may offer advantages in developing novel bioactive compounds, particularly in targeting sterically constrained binding sites. The ethylsulfanyl moiety can contribute to solubility and metabolic stability, broadening its applicability in pharmaceutical research. This compound is suited for exploratory synthesis and structure-activity relationship studies.
2-(ethylsulfanyl)spiro3.3heptane-2-carboxylic acid structure
1480448-22-3 structure
Product Name:2-(ethylsulfanyl)spiro3.3heptane-2-carboxylic acid
CAS No:1480448-22-3
MF:C10H16O2S
MW:200.297842025757
CID:5160845
PubChem ID:65131133
Update Time:2025-11-05

2-(ethylsulfanyl)spiro3.3heptane-2-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • Spiro[3.3]heptane-2-carboxylic acid, 2-(ethylthio)-
    • 2-(Ethylthio)spiro[3.3]heptane-2-carboxylic acid
    • 2-(ethylsulfanyl)spiro3.3heptane-2-carboxylic acid
    • Inchi: 1S/C10H16O2S/c1-2-13-10(8(11)12)6-9(7-10)4-3-5-9/h2-7H2,1H3,(H,11,12)
    • InChI Key: KAAWELKXEAVCOI-UHFFFAOYSA-N
    • SMILES: C1C2(CCC2)CC1(SCC)C(O)=O

2-(ethylsulfanyl)spiro3.3heptane-2-carboxylic acid Pricemore >>

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Enamine
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Additional information on 2-(ethylsulfanyl)spiro3.3heptane-2-carboxylic acid

Market Research and Analysis of 2-(ethylsulfanyl)spiro[3.3]heptane-2-carboxylic acid (1480448-22-3)

The compound 2-(ethylsulfanyl)spiro[3.3]heptane-2-carboxylic acid, identified by the CAS registry number 1480448-22-3, has garnered significant attention in the chemical and pharmaceutical industries due to its unique structural properties and potential applications in drug development. This research brief provides an in-depth analysis of the latest advancements, market demands, and supplier dynamics surrounding this compound.

Recent studies have highlighted the compound's role as a promising lead molecule in the development of novel therapeutic agents. Its spirocyclic structure and sulfur-containing functional groups contribute to its potential as a bioactive compound, particularly in anti-inflammatory and anticancer drug discovery. Researchers have demonstrated its ability to modulate key cellular pathways, making it a valuable candidate for preclinical testing.

The global market for specialty chemicals, including compounds like 1480448-22-3, is driven by increasing demand from the pharmaceutical and biotechnology sectors. The growing emphasis on personalized medicine and the need for innovative drug delivery systems have further fueled interest in this compound. Market analysis indicates a steady rise in procurement requests from academic institutions, research laboratories, and pharmaceutical companies worldwide.

Suppliers specializing in fine chemicals and intermediates play a critical role in meeting the demand for 1480448-22-3. Key players in the industry are leveraging advanced synthetic methodologies to ensure consistent quality and scalability of production. The integration of green chemistry principles has also become a priority, as companies strive to minimize environmental impact while maintaining cost efficiency.

In conclusion, 2-(ethylsulfanyl)spiro[3.3]heptane-2-carboxylic acid (1480448-22-3) represents a compelling opportunity for innovation within the chemical and pharmaceutical sectors. As research progresses and market demands evolve, collaboration between academia, industry, and suppliers will be essential to unlocking its full potential.

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