Cas no 41712-14-5 (1H-Indene-2-carboxylic acid)

1H-Indene-2-carboxylic acid is a versatile aromatic carboxylic acid derivative characterized by its fused bicyclic structure, incorporating both benzene and cyclopentene rings. This compound serves as a valuable intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its rigid indene backbone enhances structural stability, while the carboxylic acid functionality allows for further derivatization, such as esterification or amidation. The compound exhibits moderate solubility in polar organic solvents, facilitating its use in various reaction conditions. Its well-defined reactivity profile makes it suitable for applications in medicinal chemistry, where it can be employed as a building block for bioactive molecules.
1H-Indene-2-carboxylic acid structure
1H-Indene-2-carboxylic acid structure
Product Name:1H-Indene-2-carboxylic acid
CAS No:41712-14-5
MF:C10H8O2
MW:160.169322967529
MDL:MFCD00039586
CID:1037719
PubChem ID:575464
Update Time:2025-06-08

1H-Indene-2-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 1H-Indene-2-carboxylic acid
    • 2-Indencarbonsaeure
    • 2-indenecarboxylic acid
    • acide indenecarboxylique-2
    • indan-2-carboxylic acid
    • Indene-2-carboxylic acid
    • indole-2-carboxylic acid
    • BINGGEWUXWUXMJ-UHFFFAOYSA-N
    • 1H-Indene-2-carboxylicAcid
    • 5744AB
    • FCH1160781
    • TRA0074009
    • SY024866
    • DTXSID40341747
    • CS-11557
    • Z1255423596
    • AC1335
    • DA-29352
    • CS-0211365
    • InChI=1/C10H8O2/c11-10(12)9-5-7-3-1-2-4-8(7)6-9/h1-5H,6H2,(H,11,12
    • SCHEMBL1067727
    • F0001-0849
    • 41712-14-5
    • MFCD00039586
    • AKOS015840961
    • EN300-1154356
    • MDL: MFCD00039586
    • Inchi: 1S/C10H8O2/c11-10(12)9-5-7-3-1-2-4-8(7)6-9/h1-5H,6H2,(H,11,12)
    • InChI Key: BINGGEWUXWUXMJ-UHFFFAOYSA-N
    • SMILES: OC(C1=CC2C=CC=CC=2C1)=O

Computed Properties

  • Exact Mass: 160.05200
  • Monoisotopic Mass: 160.052429494g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 230
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 37.3
  • XLogP3: 2

Experimental Properties

  • PSA: 37.30000
  • LogP: 1.71070

1H-Indene-2-carboxylic acid Customs Data

  • HS CODE:2916399090
  • Customs Data:

    China Customs Code:

    2916399090

    Overview:

    2916399090 Other aromatic monocarboxylic acids. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, Acrylic acid\Acrylates or esters shall be packaged clearly

    Summary:

    2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

1H-Indene-2-carboxylic acid Pricemore >>

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1H-Indene-2-carboxylic acid Production Method

Additional information on 1H-Indene-2-carboxylic acid

Recent Advances in the Study of 1H-Indene-2-carboxylic acid (CAS: 41712-14-5) in Chemical Biology and Pharmaceutical Research

The compound 1H-Indene-2-carboxylic acid (CAS: 41712-14-5) has recently garnered significant attention in the field of chemical biology and pharmaceutical research due to its versatile chemical structure and potential therapeutic applications. This research brief aims to provide an overview of the latest studies involving this compound, highlighting its synthesis, biological activities, and potential as a drug candidate.

Recent studies have demonstrated that 1H-Indene-2-carboxylic acid serves as a key intermediate in the synthesis of various biologically active molecules. Its unique indene scaffold allows for modifications that can enhance its pharmacological properties. Researchers have explored its role in inhibiting specific enzymes involved in inflammatory pathways, making it a promising candidate for the development of anti-inflammatory drugs.

One of the groundbreaking studies published in 2023 utilized computational chemistry and molecular docking techniques to investigate the binding affinity of 1H-Indene-2-carboxylic acid with cyclooxygenase-2 (COX-2), a well-known target for anti-inflammatory drugs. The results indicated a strong interaction, suggesting its potential as a COX-2 inhibitor with fewer side effects compared to traditional nonsteroidal anti-inflammatory drugs (NSAIDs).

In addition to its anti-inflammatory properties, 1H-Indene-2-carboxylic acid has also been studied for its potential anticancer effects. A recent in vitro study demonstrated its ability to induce apoptosis in certain cancer cell lines by modulating the expression of pro-apoptotic proteins. These findings open new avenues for the development of novel anticancer therapies based on this compound.

Another area of interest is the compound's role in neurodegenerative diseases. Preliminary studies have shown that 1H-Indene-2-carboxylic acid can cross the blood-brain barrier and exhibit neuroprotective effects in models of Alzheimer's disease. Researchers are currently investigating its mechanism of action, with a focus on its ability to reduce oxidative stress and amyloid-beta aggregation.

The synthesis and optimization of 1H-Indene-2-carboxylic acid derivatives have also been a focal point of recent research. Advances in green chemistry have enabled more efficient and environmentally friendly synthesis routes, reducing the use of hazardous reagents and improving yields. These developments are crucial for scaling up production for preclinical and clinical studies.

Despite these promising findings, challenges remain in the development of 1H-Indene-2-carboxylic acid as a therapeutic agent. Issues such as bioavailability, metabolic stability, and potential toxicity need to be addressed through further research. Ongoing studies are focusing on structural modifications to enhance its pharmacokinetic properties while maintaining its biological activity.

In conclusion, 1H-Indene-2-carboxylic acid (CAS: 41712-14-5) represents a compound of significant interest in chemical biology and pharmaceutical research. Its diverse biological activities and potential therapeutic applications make it a valuable candidate for further investigation. Future research should focus on elucidating its mechanisms of action, optimizing its pharmacological properties, and advancing it through the drug development pipeline.

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