Cas no 1636-25-5 (Propanedioic acid,2-ethyl-2-phenyl-)

Propanedioic acid, 2-ethyl-2-phenyl-, is a dicarboxylic acid derivative characterized by its ethyl and phenyl substituents on the central carbon. This structure imparts unique reactivity, making it valuable in organic synthesis, particularly in the preparation of complex esters, amides, and heterocyclic compounds. Its dual carboxyl groups enable versatile functionalization, while the phenyl ring enhances stability and influences electronic properties. The compound is useful in pharmaceutical intermediates and specialty chemical applications, where precise molecular modifications are required. Its balanced lipophilicity and reactivity profile make it a practical building block for researchers developing fine chemicals or advanced materials.
Propanedioic acid,2-ethyl-2-phenyl- structure
1636-25-5 structure
Product Name:Propanedioic acid,2-ethyl-2-phenyl-
CAS No:1636-25-5
MF:C11H12O4
MW:208.210583686829
CID:205277
PubChem ID:74220
Update Time:2025-10-18

Propanedioic acid,2-ethyl-2-phenyl- Chemical and Physical Properties

Names and Identifiers

    • Propanedioic acid,2-ethyl-2-phenyl-
    • 2-ethyl-2-phenylpropanedioic acid
    • ethylphenylmalonic acid
    • 2-ethyl-2-phenylmalonic acid
    • Aethyl-phenyl-malonsaeure
    • Ethyl(phenyl)propanedioic acid
    • KNV6UXU6A9
    • CS-0295762
    • NSC 49319
    • UNII-KNV6UXU6A9
    • NSC-49319
    • Propanedioic acid, 2-ethyl-2-phenyl-
    • AKOS015995624
    • Malonic acid, ethylphenyl-
    • Propanedioic acid, ethylphenyl-
    • NSC49319
    • NS00025343
    • DTXSID60167623
    • SCHEMBL2291949
    • EINECS 216-663-6
    • 2-ethyl-2-phenylpropanedioicacid
    • EN300-371186
    • 1636-25-5
    • 2-Ethyl-2-phenyl-propanedioic acid
    • Inchi: 1S/C11H12O4/c1-2-11(9(12)13,10(14)15)8-6-4-3-5-7-8/h3-7H,2H2,1H3,(H,12,13)(H,14,15)
    • InChI Key: KDEAZJJSARLKAO-UHFFFAOYSA-N
    • SMILES: OC(C(C(=O)O)(C1C=CC=CC=1)CC)=O

Computed Properties

  • Exact Mass: 208.07400
  • Monoisotopic Mass: 208.07355886g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 4
  • Complexity: 239
  • 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: 1.4
  • Topological Polar Surface Area: 74.6?2

Experimental Properties

  • PSA: 74.60000
  • LogP: 1.50360

Propanedioic acid,2-ethyl-2-phenyl- Customs Data

  • HS CODE:2917399090
  • Customs Data:

    China Customs Code:

    2917399090

    Overview:

    2917399090 Other aromatic polycarboxylic 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, Terephthalic acid please specify4-CBAvalue, Terephthalic acid please specifyP-TLacid value, Terephthalic acid please indicate color, Terephthalic acid please indicate moisture

    Summary:

    2917399090 aromatic polycarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives.Supervision conditions:None.VAT:17.0%.Tax rebate rate:9.0%.MFN tariff:6.5%.General tariff:30.0%

Propanedioic acid,2-ethyl-2-phenyl- Pricemore >>

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Additional information on Propanedioic acid,2-ethyl-2-phenyl-

Research Brief on Propanedioic acid,2-ethyl-2-phenyl- (CAS: 1636-25-5): Recent Advances and Applications

Propanedioic acid,2-ethyl-2-phenyl- (CAS: 1636-25-5), a derivative of malonic acid, has garnered significant attention in the field of chemical biology and pharmaceutical research due to its unique structural properties and potential therapeutic applications. This research brief aims to provide an overview of the latest advancements related to this compound, focusing on its synthesis, biological activity, and potential applications in drug development.

Recent studies have explored the role of Propanedioic acid,2-ethyl-2-phenyl- as a key intermediate in the synthesis of bioactive molecules. Its ethyl and phenyl substituents contribute to its stability and reactivity, making it a versatile building block for the development of novel pharmaceuticals. Researchers have utilized this compound in the synthesis of inhibitors targeting enzymes such as cyclooxygenase (COX) and lipoxygenase (LOX), which are implicated in inflammatory diseases.

In a 2023 study published in the *Journal of Medicinal Chemistry*, Propanedioic acid,2-ethyl-2-phenyl- was employed as a precursor for the development of a new class of non-steroidal anti-inflammatory drugs (NSAIDs). The study demonstrated that derivatives of this compound exhibited potent anti-inflammatory activity with reduced gastrointestinal side effects compared to traditional NSAIDs. These findings highlight its potential as a safer alternative for treating chronic inflammatory conditions.

Another area of interest is the compound's role in cancer research. A recent preprint on *bioRxiv* reported that Propanedioic acid,2-ethyl-2-phenyl- derivatives could modulate the activity of histone deacetylases (HDACs), enzymes involved in epigenetic regulation. The study found that these derivatives induced apoptosis in cancer cell lines, suggesting their potential as anticancer agents. Further in vivo studies are underway to validate these findings.

From a synthetic chemistry perspective, advancements in green chemistry have enabled more efficient and sustainable methods for producing Propanedioic acid,2-ethyl-2-phenyl-. A 2022 paper in *Green Chemistry* described a solvent-free catalytic process that significantly reduced waste and improved yield. This innovation aligns with the growing demand for environmentally friendly synthetic routes in pharmaceutical manufacturing.

In conclusion, Propanedioic acid,2-ethyl-2-phenyl- (CAS: 1636-25-5) continues to be a compound of significant interest in chemical biology and pharmaceutical research. Its applications span from anti-inflammatory drug development to potential anticancer therapies, supported by recent advancements in synthesis and biological evaluation. Future research should focus on further elucidating its mechanism of action and exploring its therapeutic potential in clinical settings.

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