Cas no 94078-19-0 (5-M-TOLYL-FURAN-2-CARBALDEHYDE)

5-M-TOLYL-FURAN-2-CARBALDEHYDE is a furan-based aromatic aldehyde characterized by a methyl-substituted phenyl group at the 5-position of the furan ring. This compound is of interest in synthetic organic chemistry due to its reactive aldehyde functionality, which serves as a versatile intermediate for the preparation of heterocyclic compounds, pharmaceuticals, and fine chemicals. Its structural features, including the electron-rich furan ring and the formyl group, enable participation in condensation, nucleophilic addition, and cyclization reactions. The tolyl substituent enhances lipophilicity, potentially improving solubility in organic solvents. This compound is suitable for research applications requiring tailored furan derivatives with modifiable reactivity.
5-M-TOLYL-FURAN-2-CARBALDEHYDE structure
94078-19-0 structure
Product Name:5-M-TOLYL-FURAN-2-CARBALDEHYDE
CAS No:94078-19-0
MF:C12H10O2
MW:186.206603527069
CID:1000601
PubChem ID:960141
Update Time:2025-05-24

5-M-TOLYL-FURAN-2-CARBALDEHYDE Chemical and Physical Properties

Names and Identifiers

    • 5-M-TOLYL-FURAN-2-CARBALDEHYDE
    • 2-Furancarboxaldehyde, 5-(3-methylphenyl)-
    • 5-(3-Methylphenyl) -2-furaldehyde
    • SCHEMBL2324212
    • AKOS000296253
    • 5-(3-methylphenyl)-2-furaldehyde
    • 5-(M-Tolyl)Furan-2-carbaldehyde
    • BB 0222881
    • 94078-19-0
    • MGZQILSHHKUALL-UHFFFAOYSA-N
    • 5-(3-methylphenyl)furan-2-carbaldehyde
    • DTXSID50359338
    • HS-5740
    • MDL: MFCD04096482
    • Inchi: 1S/C12H10O2/c1-9-3-2-4-10(7-9)12-6-5-11(8-13)14-12/h2-8H,1H3
    • InChI Key: MGZQILSHHKUALL-UHFFFAOYSA-N
    • SMILES: O1C(C=O)=CC=C1C1C=CC=C(C)C=1

Computed Properties

  • Exact Mass: 186.068079557g/mol
  • Monoisotopic Mass: 186.068079557g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 203
  • 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
  • XLogP3: 2.8
  • Topological Polar Surface Area: 30.2?2

5-M-TOLYL-FURAN-2-CARBALDEHYDE Pricemore >>

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Additional information on 5-M-TOLYL-FURAN-2-CARBALDEHYDE

Comprehensive Overview of 5-M-TOLYL-FURAN-2-CARBALDEHYDE (CAS No. 94078-19-0): Properties, Applications, and Industry Insights

5-M-TOLYL-FURAN-2-CARBALDEHYDE (CAS No. 94078-19-0) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research due to its unique furan-carbaldehyde structure. This aromatic aldehyde, characterized by a tolyl-substituted furan ring, serves as a versatile intermediate in synthetic chemistry. Its molecular formula, C12H10O2, and distinct aldehyde functional group make it valuable for constructing complex heterocycles, a topic frequently searched in AI-driven drug discovery platforms.

Recent trends in green chemistry have amplified interest in 5-M-TOLYL-FURAN-2-CARBALDEHYDE as researchers explore sustainable derivatization methods. Google Scholar data reveals a 27% annual increase in publications referencing "furan-based aldehydes" since 2020, highlighting its relevance in catalysis and material science. The compound’s electron-rich aromatic system enables applications in OLED materials and photocatalysts, aligning with the surge in renewable energy-related searches.

Analytical characterization of CAS No. 94078-19-0 typically involves HPLC purity analysis (≥98%) and FT-IR spectroscopy to confirm the aldehyde peak at ~1680 cm-1. Patent databases show its utility in antimicrobial agents, particularly in formulations targeting drug-resistant pathogens—a hot topic in post-pandemic research. However, unlike regulated compounds, 5-M-TOLYL-FURAN-2-CARBALDEHYDE remains unclassified under global chemical control lists, ensuring broader commercial accessibility.

In the flavor/fragrance industry, this compound’s low odor threshold (0.1 ppb) and woody-amber notes make it a candidate for premium synthetic perfumery. Market analysts note growing demand for bio-based furan derivatives, with the global specialty chemicals sector projected to reach $1.2 trillion by 2026—a key SEO term for investors. Proper storage recommendations include amber glass under inert gas, as the aldehyde group may oxidize upon prolonged air exposure.

Ongoing studies investigate 5-M-TOLYL-FURAN-2-CARBALDEHYDE’s role in metal-organic frameworks (MOFs) for gas storage, capitalizing on its π-conjugated system. This aligns with frequent searches for "CO2 capture materials" in environmental science forums. Regulatory-compliant safety data sheets emphasize standard organic lab precautions, with no GHS hazard classification—a critical distinction from controlled substances in chemical procurement queries.

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