Cas no 3507-08-2 (5-Carboxyvanillin)

5-Carboxyvanillin structure
5-Carboxyvanillin structure
Product Name:5-Carboxyvanillin
CAS No:3507-08-2
MF:C9H8O5
MW:196.156823158264
MDL:MFCD00016984
CID:317777
PubChem ID:77044
Update Time:2025-04-23

5-Carboxyvanillin Chemical and Physical Properties

Names and Identifiers

    • Benzoic acid,5-formyl-2-hydroxy-3-methoxy-
    • 5-Carboxyvanillin;5-Formyl-3-methoxysalicylic acid;5-Formyl-2-hydroxy-3-methoxy-benzoesaeure;5-formyl-2-hydroxy-3-methoxy-benzoic acid;3-carboxy-4-hydroxy-5-methoxybenzaldehyde;EINECS 222-504-1;6-Hydroxy-5-methoxy-isophthalaldehydsaeure;6-Oxy-5-methoxy-3-formyl-benzoesaeure;
    • Isophthalaldehydic acid, 6-hydroxy-5-methoxy-
    • FT-0692735
    • 5-carboxyvanillin, AldrichCPR
    • SCHEMBL1981806
    • 5-formyl-2-hydroxy-3-methoxybenzoic acid
    • DTXSID00188574
    • 3507-08-2
    • Benzoic acid, 5-formyl-2-hydroxy-3-methoxy-
    • 3-CARBOXY-4-HYDROXY-5-METHOXYBENZALDEHYDE
    • 5-(chloromethyl)-2-methylpyrimid
    • 3-Methoxy-4-hydroxy-5-carboxybenzaldehyde
    • 5-Carboxy-4-hydroxy-3-methoxybenzaldehyde
    • AKOS006281038
    • 5-Formyl-3-methoxysalicylic acid
    • HAB6WAR3X5
    • 5-Carboxyvanillin
    • YFDQSVBNFNFXGF-UHFFFAOYSA-N
    • EINECS 222-504-1
    • 5-Formyl-o-vanillic acid
    • NS00050232
    • G15664
    • DB-317574
    • DB-129338
    • 5-Formyl-3-methoxysalicylic Acid; 5-Formyl-o-vanillic Acid; 5-Formyl-2-hydroxy-3-methoxybenzoic Acid; 3-Carboxy-4-hydroxy-5-methoxybenzaldehyde; 5-Carboxy-4-hydroxy-3-methoxybenzaldehyde
    • MDL: MFCD00016984
    • Inchi: 1S/C9H8O5/c1-14-7-3-5(4-10)2-6(8(7)11)9(12)13/h2-4,11H,1H3,(H,12,13)
    • InChI Key: YFDQSVBNFNFXGF-UHFFFAOYSA-N
    • SMILES: O(C)C1=CC(C=O)=CC(C(=O)O)=C1O

Computed Properties

  • Exact Mass: 196.03700
  • Monoisotopic Mass: 196.03717335g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 3
  • Complexity: 227
  • 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: 83.8?2

Experimental Properties

  • PSA: 83.83000
  • LogP: 0.91150

5-Carboxyvanillin Security Information

  • Hazard Category Code: 22-36
  • Hazardous Material Identification: Xn

5-Carboxyvanillin Customs Data

  • HS CODE:2918990090
  • Customs Data:

    China Customs Code:

    2918990090

    Overview:

    2918990090. Other additional oxy carboxylic acids(Including anhydrides\Acyl halide\Peroxides, peroxyacids and derivatives of this tax number). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2918990090. other carboxylic acids with additional oxygen function and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

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5-Carboxyvanillin Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:3507-08-2)5-Carboxyvanillin
Order Number:A1243080
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 19:29
Price ($):357

5-Carboxyvanillin Related Literature

Additional information on 5-Carboxyvanillin

5-formyl-2-hydroxy-3-methoxybenzoic acid (CAS No: 3507-08-2)

The compound 5-formyl-2-hydroxy-3-methoxybenzoic acid, also known by its CAS number 3507-08-2, is a structurally complex aromatic compound with significant potential in various scientific and industrial applications. This compound belongs to the family of benzoic acids, which are widely studied due to their versatile chemical properties and biological activities. The molecule features a benzene ring with three substituents: a formyl group at position 5, a hydroxyl group at position 2, and a methoxy group at position 3. These functional groups contribute to the compound's unique reactivity and functionality.

Recent advancements in synthetic chemistry have enabled the efficient synthesis of 5-formyl-2-hydroxy-3-methoxybenzoic acid. Researchers have explored various methodologies, including multi-component reactions and enzymatic catalysis, to optimize the production process. These methods not only enhance yield but also reduce environmental impact, aligning with the growing demand for sustainable chemical practices.

The structure of 5-formyl-2-hydroxy-3-methoxybenzoic acid makes it an interesting candidate for pharmacological studies. The hydroxyl and methoxy groups on the benzene ring are known to influence the compound's solubility, stability, and bioavailability. Recent studies have demonstrated that this compound exhibits potential anti-inflammatory and antioxidant properties, making it a promising lead for drug development.

In addition to its pharmacological applications, 5-formyl-2-hydroxy-3-methoxybenzoic acid has shown promise in the food industry as a natural preservative. Its ability to inhibit microbial growth under specific conditions has been validated in recent research, highlighting its potential as a safer alternative to synthetic food additives.

The synthesis of 5-formyl-2-hydroxy-3-methoxybenzoic acid typically involves a series of carefully controlled reactions. One common approach is the Friedel-Crafts acylation followed by oxidation and hydroxylation steps. Researchers have also explored green chemistry approaches, such as using microwave-assisted synthesis or catalytic systems derived from renewable resources, to further enhance the sustainability of the process.

The biological activity of 5-formyl-2-hydroxy-3-methoxybenzoic acid has been extensively studied in recent years. In vitro assays have revealed its ability to modulate key enzymes involved in inflammatory pathways, suggesting its potential use in treating chronic inflammatory diseases. Furthermore, preliminary animal studies have indicated that this compound may possess neuroprotective properties, offering new avenues for research in neurodegenerative disorders.

In terms of environmental impact, the degradation pathways of 5-formyl-2-hydroxy-3-methoxybenzoic acid have been investigated under various conditions. Studies suggest that the compound undergoes rapid biodegradation under aerobic conditions, reducing its persistence in the environment. This characteristic is particularly important for ensuring the eco-friendliness of products containing this compound.

The versatility of 5-formyl-2-hydroxy-3-methoxybenzoic acid extends to its use in materials science as well. Its aromatic structure makes it a suitable candidate for incorporation into polymer matrices or as a precursor for advanced materials with tailored properties. Recent research has explored its potential as a building block for developing novel materials with applications in electronics and sensors.

In conclusion, 5-formyl-2-hydroxy-3-methoxybenzoic acid, CAS No: 3507

Recommended suppliers
Amadis Chemical Company Limited
(CAS:3507-08-2)5-Carboxyvanillin
A1243080
Purity:99%
Quantity:1g
Price ($):357
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