Cas no 893737-63-8 (2-hydroxy-5-(2-methoxyphenyl)benzaldehyde)

2-Hydroxy-5-(2-methoxyphenyl)benzaldehyde is a versatile aromatic aldehyde featuring both hydroxyl and methoxy functional groups, which enhance its reactivity and utility in organic synthesis. The compound’s structure, combining a benzaldehyde core with a substituted phenyl ring, makes it a valuable intermediate for pharmaceuticals, agrochemicals, and fine chemicals. Its ortho-hydroxyl group facilitates chelation and further functionalization, while the methoxy substituent influences electronic properties, enabling selective reactions. This compound is particularly useful in the synthesis of complex molecules, including ligands and heterocycles, due to its balanced steric and electronic effects. High purity and stability under standard conditions further support its application in research and industrial processes.
2-hydroxy-5-(2-methoxyphenyl)benzaldehyde structure
893737-63-8 structure
Product Name:2-hydroxy-5-(2-methoxyphenyl)benzaldehyde
CAS No:893737-63-8
MF:C14H12O3
MW:228.243284225464
MDL:MFCD06802116
CID:1941296
PubChem ID:20099796
Update Time:2025-11-02

2-hydroxy-5-(2-methoxyphenyl)benzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde
    • 4-HYDROXY-2'-METHOXY[1,1'-BIPHENYL]-3-CARBALDEHYDE
    • 2-Formyl-4-(2-methoxyphenyl)phenol
    • MFCD06802116
    • 2-Formyl-4-(2-methoxyphenyl)phenol, 95%
    • DTXSID00602402
    • 893737-63-8
    • A1-53771
    • AKOS004116120
    • SCHEMBL12833545
    • 4-Hydroxy-2'-methoxy-[1,1'-biphenyl]-3-carbaldehyde
    • MDL: MFCD06802116
    • Inchi: 1S/C14H12O3/c1-17-14-5-3-2-4-12(14)10-6-7-13(16)11(8-10)9-15/h2-9,16H,1H3
    • InChI Key: VHRAILLXUOZKTO-UHFFFAOYSA-N
    • SMILES: O(C)C1C=CC=CC=1C1C=CC(=C(C=O)C=1)O

Computed Properties

  • Exact Mass: 228.078644241Da
  • Monoisotopic Mass: 228.078644241Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 3
  • Complexity: 254
  • 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: 3.2
  • Topological Polar Surface Area: 46.5?2

2-hydroxy-5-(2-methoxyphenyl)benzaldehyde Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB320722-5 g
2-Formyl-4-(2-methoxyphenyl)phenol, 95%; .
893737-63-8 95%
5g
€1159.00 2023-04-26
abcr
AB320722-5g
2-Formyl-4-(2-methoxyphenyl)phenol, 95%; .
893737-63-8 95%
5g
€1159.00 2025-04-15

Additional information on 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde

2-Hydroxy-5-(2-methoxyphenyl)benzaldehyde: A Versatile Chemical Intermediate with Emerging Applications

The compound 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde (CAS No. 893737-63-8) represents an important class of aromatic aldehydes that has gained significant attention in recent years due to its unique structural features and broad utility in organic synthesis. This hydroxy-methoxy benzaldehyde derivative serves as a valuable building block for the preparation of various pharmacologically active compounds, functional materials, and specialty chemicals.

Chemically classified as a benzaldehyde derivative, this compound features a hydroxyl group at the 2-position and a methoxyphenyl substituent at the 5-position of the benzaldehyde core. The presence of these functional groups makes 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde particularly interesting for synthetic applications, as it offers multiple sites for chemical modification. The CAS 893737-63-8 compound has become increasingly relevant in pharmaceutical research, where researchers are exploring its potential as a precursor for novel drug candidates.

Recent studies have highlighted the importance of hydroxy-substituted benzaldehydes in medicinal chemistry, particularly in the development of antioxidant and anti-inflammatory agents. The structural motif present in 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde is similar to that found in many natural products with biological activity, making it a valuable scaffold for drug discovery. This connection to natural product chemistry has driven increased interest in the compound, as evidenced by rising search volumes for terms like "hydroxy benzaldehyde derivatives" and "methoxyphenyl aldehyde applications" across scientific databases.

The synthesis of CAS 893737-63-8 typically involves well-established organic transformations, with researchers continuously optimizing production methods to improve yield and purity. Modern synthetic approaches often employ green chemistry principles, addressing the growing demand for sustainable chemical processes. This aligns with current industry trends toward environmentally friendly synthesis methods, a topic that frequently appears in searches related to "green synthesis of aromatic aldehydes" and "sustainable production of benzaldehyde derivatives."

In material science applications, 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde has shown promise as a precursor for functional polymers and coordination compounds. Its ability to form stable complexes with various metal ions makes it particularly valuable for creating advanced materials with specific optical or electronic properties. Recent patent literature reveals growing interest in these applications, with search terms like "benzaldehyde-based materials" and "hydroxy aldehyde polymers" gaining traction among researchers.

The compound's physicochemical properties, including its melting point, solubility characteristics, and spectral properties, have been well-documented in the scientific literature. These properties make 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde particularly suitable for various analytical applications, where it may serve as a reference standard or derivatization reagent. The increasing demand for high-purity chemical standards is reflected in search queries such as "analytical grade benzaldehydes" and "reference standards for aldehyde analysis."

Quality control aspects of CAS 893737-63-8 production have become increasingly important, particularly for pharmaceutical applications. Modern analytical techniques including HPLC, GC-MS, and NMR spectroscopy are routinely employed to ensure the compound meets stringent purity requirements. This focus on quality aligns with industry-wide trends toward stricter regulatory standards, a topic frequently searched as "pharmaceutical intermediate purity standards" and "analytical methods for aldehyde compounds."

From a commercial perspective, the market for hydroxy-methoxy benzaldehyde derivatives has shown steady growth, driven by expanding applications in multiple industries. Suppliers and manufacturers have responded to this demand by improving production scalability and developing specialized grades of the compound. Business-related searches such as "2-hydroxy-5-(2-methoxyphenyl)benzaldehyde suppliers" and "bulk benzaldehyde derivatives" indicate strong commercial interest in this chemical intermediate.

Looking forward, research into 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde continues to uncover new potential applications. Recent studies have explored its use in asymmetric synthesis, catalysis, and as a ligand in coordination chemistry. These developments correspond with growing academic interest, as shown by increasing citations in peer-reviewed journals and search terms like "benzaldehyde derivatives in catalysis" and "asymmetric synthesis using aromatic aldehydes."

Safety considerations for handling CAS 893737-63-8 follow standard laboratory practices for aromatic aldehydes. While not classified as hazardous under most regulatory frameworks, proper handling procedures should always be followed. This practical aspect generates consistent search interest, with queries such as "handling aromatic aldehydes safely" and "storage conditions for benzaldehyde derivatives" appearing regularly in safety-related searches.

The future outlook for 2-hydroxy-5-(2-methoxyphenyl)benzaldehyde appears promising, with potential applications continuing to emerge across diverse scientific disciplines. As research into functionalized aromatic compounds advances, this versatile intermediate is likely to maintain its importance in both academic and industrial settings. The compound's unique combination of reactivity and stability ensures its ongoing relevance in chemical synthesis and materials development.

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