Cas no 75002-34-5 (2,4-dimethyl-3-furaldehyde)

2,4-Dimethyl-3-furaldehyde is a furan-based aldehyde compound characterized by its distinct aromatic properties and reactivity. This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the production of flavor and fragrance compounds due to its unique organoleptic profile. Its molecular structure, featuring methyl substituents at the 2- and 4-positions, enhances stability while maintaining reactivity at the aldehyde functional group. The compound is valued for its role in heterocyclic chemistry, enabling the synthesis of complex furan derivatives. It is commonly employed in research and industrial applications where controlled functionalization of furan rings is required. Proper handling is essential due to its sensitivity to light and air.
2,4-dimethyl-3-furaldehyde structure
2,4-dimethyl-3-furaldehyde structure
Product Name:2,4-dimethyl-3-furaldehyde
CAS No:75002-34-5
MF:C7H8O2
MW:124.137222290039
CID:557725
PubChem ID:21702758
Update Time:2025-06-14

2,4-dimethyl-3-furaldehyde Chemical and Physical Properties

Names and Identifiers

    • 3-Furancarboxaldehyde,2,4-dimethyl-
    • 2,4-dimethylfuran-3-carbaldehyde
    • 3-Furancarboxaldehyde, 2,4-dimethyl- (9CI)
    • 2,4-Dimethyl-3-furaldehyde
    • 2,4-dimethyl-furan-3-carbaldehyde
    • 3-furancarbaldehyde,2,4-dimethyl
    • 3-Furancarboxaldehyde,2,4-dimethyl
    • 75002-34-5
    • DTXSID60617138
    • starbld0004407
    • AKOS006334150
    • SCHEMBL3261425
    • MS-22595
    • FT-0724108
    • DB-074933
    • 2,4-dimethyl-3-furaldehyde
    • Inchi: 1S/C7H8O2/c1-5-4-9-6(2)7(5)3-8/h3-4H,1-2H3
    • InChI Key: MGSAYHDYMMHZQE-UHFFFAOYSA-N
    • SMILES: O1C=C(C)C(C=O)=C1C

Computed Properties

  • Exact Mass: 124.05200
  • Monoisotopic Mass: 124.052429494g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 112
  • 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: 1.2
  • Topological Polar Surface Area: 30.2?2

Experimental Properties

  • PSA: 30.21000
  • LogP: 1.70890

2,4-dimethyl-3-furaldehyde Customs Data

  • HS CODE:2932190090
  • Customs Data:

    China Customs Code:

    2932190090

    Overview:

    2932190090 Other structurally non fused furan ring compounds. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2932190090 other compounds containing an unfused furan ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

2,4-dimethyl-3-furaldehyde Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
D478605-10mg
2,4-dimethyl-3-furaldehyde
75002-34-5
10mg
$ 50.00 2022-06-05
TRC
D478605-50mg
2,4-dimethyl-3-furaldehyde
75002-34-5
50mg
$ 115.00 2022-06-05
TRC
D478605-100mg
2,4-dimethyl-3-furaldehyde
75002-34-5
100mg
$ 185.00 2022-06-05
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1660266-250mg
2,4-Dimethylfuran-3-carbaldehyde
75002-34-5 98%
250mg
¥973.00 2024-04-30
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1660266-1g
2,4-Dimethylfuran-3-carbaldehyde
75002-34-5 98%
1g
¥16999.00 2024-07-28

2,4-dimethyl-3-furaldehyde Related Literature

Additional information on 2,4-dimethyl-3-furaldehyde

Recent Advances in the Study of 2,4-Dimethyl-3-furaldehyde (CAS: 75002-34-5) in Chemical Biology and Pharmaceutical Research

2,4-Dimethyl-3-furaldehyde (CAS: 75002-34-5) is a furan derivative that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This compound, characterized by its unique structural features, has been explored for its reactivity, biological activity, and utility as a building block in synthetic chemistry. Recent studies have shed light on its role in drug discovery, flavor and fragrance chemistry, and material science, making it a compound of considerable interest to researchers in these fields.

One of the most notable aspects of 2,4-dimethyl-3-furaldehyde is its role as an intermediate in the synthesis of more complex molecules. Recent research has demonstrated its utility in the construction of heterocyclic compounds, which are pivotal in medicinal chemistry. For instance, a 2023 study published in the Journal of Medicinal Chemistry highlighted its use in the synthesis of novel antimicrobial agents, where the furan ring served as a key pharmacophore. The study reported that derivatives of 2,4-dimethyl-3-furaldehyde exhibited promising activity against a range of Gram-positive and Gram-negative bacteria, suggesting its potential as a scaffold for developing new antibiotics.

In addition to its pharmaceutical applications, 2,4-dimethyl-3-furaldehyde has been investigated for its flavor and fragrance properties. A recent study in Flavour and Fragrance Journal (2024) explored its contribution to the aroma profiles of various food products. The researchers identified that this compound imparts a sweet, caramel-like odor, making it a valuable ingredient in the flavor industry. The study also emphasized the need for further research into its safety and regulatory status, as its use in food products is still under scrutiny.

From a mechanistic standpoint, the reactivity of 2,4-dimethyl-3-furaldehyde has been a focal point of recent investigations. A 2023 paper in Organic Letters detailed its participation in [4+2] cycloaddition reactions, which are instrumental in the synthesis of complex organic frameworks. The study provided insights into the compound's electronic properties and its ability to act as a diene or dienophile, depending on the reaction conditions. These findings have important implications for the design of new synthetic methodologies in organic chemistry.

Despite these advancements, challenges remain in the large-scale production and application of 2,4-dimethyl-3-furaldehyde. A 2024 review in Chemical Reviews highlighted the need for more sustainable and efficient synthetic routes to this compound, as current methods often involve hazardous reagents or low yields. The review also called for more comprehensive toxicological studies to ensure its safe use in pharmaceutical and consumer products.

In conclusion, 2,4-dimethyl-3-furaldehyde (CAS: 75002-34-5) continues to be a compound of significant interest in chemical biology and pharmaceutical research. Its diverse applications, from drug discovery to flavor chemistry, underscore its versatility and potential. Future research should focus on addressing the existing challenges related to its synthesis and safety, paving the way for its broader adoption in industry and academia.

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