Cas no 73220-20-9 (Benzaldehyde, 5-methoxy-2-(methoxymethoxy)-)

Benzaldehyde, 5-methoxy-2-(methoxymethoxy)-, is a specialized aromatic aldehyde featuring methoxy and methoxymethoxy substituents at the 5- and 2-positions, respectively. This compound is of interest in synthetic organic chemistry due to its electron-rich aromatic system, which enhances reactivity in electrophilic substitution and condensation reactions. The methoxymethoxy group offers additional functionalization potential, serving as a protected hydroxyl equivalent that can be deprotected under mild conditions. Its structural features make it a valuable intermediate in the synthesis of pharmaceuticals, fragrances, and fine chemicals. The compound's stability and well-defined reactivity profile ensure consistent performance in multi-step synthetic routes.
Benzaldehyde, 5-methoxy-2-(methoxymethoxy)- structure
73220-20-9 structure
Product Name:Benzaldehyde, 5-methoxy-2-(methoxymethoxy)-
CAS No:73220-20-9
MF:C10H12O4
MW:196.199883460999
CID:1765224
PubChem ID:11435522
Update Time:2025-05-22

Benzaldehyde, 5-methoxy-2-(methoxymethoxy)- Chemical and Physical Properties

Names and Identifiers

    • Benzaldehyde, 5-methoxy-2-(methoxymethoxy)-
    • 5-methoxy-2-(methoxymethoxy)Benzaldehyde
    • SCHEMBL3221472
    • WSMHWPOBGUNBJR-UHFFFAOYSA-N
    • 5-methoxy-2-methoxymethoxybenzaldehyde
    • AKOS014699969
    • Z1259227427
    • 73220-20-9
    • G60008
    • DA-20146
    • CS-0223282
    • DTXSID40465755
    • EN300-114617
    • Inchi: 1S/C10H12O4/c1-12-7-14-10-4-3-9(13-2)5-8(10)6-11/h3-6H,7H2,1-2H3
    • InChI Key: WSMHWPOBGUNBJR-UHFFFAOYSA-N
    • SMILES: O(COC)C1C=CC(=CC=1C=O)OC

Computed Properties

  • Exact Mass: 196.07355886g/mol
  • Monoisotopic Mass: 196.07355886g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 5
  • Complexity: 172
  • 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: 1.3
  • Topological Polar Surface Area: 44.8?2

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Additional information on Benzaldehyde, 5-methoxy-2-(methoxymethoxy)-

Benzaldehyde, 5-methoxy-2-(methoxymethoxy) (CAS No.73220-20-9)

Benzaldehyde, 5-methoxy-2-(methoxymethoxy), also known by its CAS registry number CAS No.73220-20-9, is a versatile organic compound with significant applications in various fields of chemistry and pharmacology. This compound belongs to the class of aromatic aldehydes, characterized by the presence of a benzene ring with an aldehyde group and specific substituents. The structure of this compound includes a methoxy group at the 5-position and a methoxymethoxy group at the 2-position of the benzene ring, which imparts unique chemical properties and reactivity.

The synthesis of Benzaldehyde, 5-methoxy-2-(methoxymethoxy) typically involves multi-step organic reactions, often utilizing protection and deprotection strategies to achieve the desired substitution pattern on the benzene ring. Recent advancements in catalytic methods and green chemistry have enabled more efficient and environmentally friendly syntheses of this compound, reducing the overall environmental footprint while maintaining high yields and purity.

In terms of applications, Benzaldehyde, 5-methoxy-2-(methoxymethoxy) has found significant use in the pharmaceutical industry as an intermediate in drug development. Its unique substitution pattern makes it an ideal candidate for exploring novel drug delivery systems and targeted therapies. For instance, researchers have employed this compound as a precursor for synthesizing bioactive molecules with potential anti-inflammatory, antioxidant, and anticancer properties.

Recent studies have highlighted the role of Benzaldehyde, 5-methoxy-2-(methoxymethoxy) in medicinal chemistry as a building block for constructing complex molecular architectures. Its ability to undergo various functional group transformations has made it a valuable tool in combinatorial chemistry and high-throughput screening campaigns. Additionally, this compound has been utilized in the development of advanced materials, including stimuli-responsive polymers and nanomaterials.

The chemical stability of Benzaldehyde, 5-methoxy-2-(methoxymethoxy) is another critical aspect that has been extensively studied. Under normal storage conditions, this compound exhibits good stability; however, exposure to light or elevated temperatures may lead to degradation products. Understanding these degradation pathways is crucial for ensuring the quality and safety of products derived from this compound.

In terms of environmental impact, recent research has focused on assessing the biodegradability and eco-toxicological effects of Benzaldehyde, 5-methoxy-2-(methoxymethoxy). Studies indicate that under aerobic conditions, this compound can undergo microbial degradation; however, its persistence in aquatic environments remains a concern requiring further investigation.

The future outlook for Benzaldehyde, 5-methoxy-2-(methoxymethoxy) is promising, with ongoing research exploring its potential in emerging areas such as bioinformatics and personalized medicine. Its role as a key intermediate in drug discovery pipelines positions it as an essential component in advancing therapeutic solutions for various diseases.

In conclusion, Benzaldehyde, 5-methoxy-2-(methoxymethoxy) (CAS No.73220-20-9) is a multifaceted organic compound with diverse applications across multiple disciplines. Its unique chemical properties make it an invaluable tool in both academic research and industrial applications. As scientific advancements continue to unfold, this compound is expected to play an even more pivotal role in shaping innovative solutions across various sectors.

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