Cas no 898289-31-1 (Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]-)

Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- is a specialized aromatic aldehyde derivative featuring a tetrahydro-2H-pyran-4-yloxy substituent at the ortho position of the benzaldehyde core. This compound exhibits unique reactivity due to the electron-donating effect of the ether linkage and the steric influence of the tetrahydropyran ring, making it valuable in asymmetric synthesis and pharmaceutical intermediates. The tetrahydropyran moiety enhances solubility in organic solvents while maintaining stability under various reaction conditions. Its structural features make it particularly useful in palladium-catalyzed cross-coupling reactions and as a precursor for chiral ligands. The compound's purity (>97% by GC) and well-defined stereochemistry allow for precise applications in complex molecule construction.
Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- structure
898289-31-1 structure
Product Name:Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]-
CAS No:898289-31-1
MF:C12H14O3
MW:206.237763881683
CID:719788
PubChem ID:18936058
Update Time:2025-11-01

Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- Chemical and Physical Properties

Names and Identifiers

    • Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]-
    • 2-(oxan-4-yloxy)benzaldehyde
    • 2-(Tetrahydro-2H-pyran-4-yloxy)benzaldehyde
    • 2-(tetrahydropyran-4-yloxy)benzaldehyde
    • DTXSID00596650
    • YKB28931
    • 2-((Tetrahydro-2H-pyran-4-yl)oxy)benzaldehyde
    • FT-0737695
    • 898289-31-1
    • PS-5361
    • AMY5007
    • MFCD09064958
    • 2-[(Oxan-4-yl)oxy]benzaldehyde
    • AKOS013153988
    • SCHEMBL8115816
    • CS-0459348
    • DB-078509
    • G88830
    • Inchi: 1S/C12H14O3/c13-9-10-3-1-2-4-12(10)15-11-5-7-14-8-6-11/h1-4,9,11H,5-8H2
    • InChI Key: UCRWIPOHJNTVKS-UHFFFAOYSA-N
    • SMILES: O1CCC(CC1)OC1C=CC=CC=1C=O

Computed Properties

  • Exact Mass: 206.09400
  • Monoisotopic Mass: 206.094294304g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 3
  • Complexity: 199
  • 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: 2.1
  • Topological Polar Surface Area: 35.5?2

Experimental Properties

  • Density: 1.154
  • Melting Point: 67-70
  • Boiling Point: 349.1°C at 760 mmHg
  • Flash Point: 156.2°C
  • Refractive Index: 1.559
  • PSA: 35.53000
  • LogP: 2.05690

Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- Security Information

Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- Pricemore >>

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Additional information on Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]-

Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- (CAS No. 898289-31-1): A Versatile Intermediate in Modern Organic Synthesis

The compound Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- (CAS No. 898289-31-1) is a highly specialized aromatic aldehyde derivative that has garnered significant attention in the field of organic chemistry and pharmaceutical research. Its unique molecular structure, featuring a tetrahydro-2H-pyran-4-yl ether linkage, makes it a valuable building block for the synthesis of complex molecules. This article delves into the properties, applications, and recent advancements related to this compound, addressing common queries such as "What is Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- used for?" and "How is CAS 898289-31-1 synthesized?".

One of the key features of Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- is its role as a protected aldehyde intermediate. The tetrahydro-2H-pyran-4-yl group acts as a protective moiety, shielding the reactive aldehyde functionality during multi-step synthetic processes. This property is particularly valuable in the production of flavorants, fragrances, and pharmaceutical intermediates, where selective reactivity is crucial. Recent studies have highlighted its utility in the synthesis of chiral compounds, addressing the growing demand for enantioselective transformations in drug development.

In the context of green chemistry trends, researchers are exploring eco-friendly synthetic routes for CAS 898289-31-1. Questions like "Is there a sustainable method to produce Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]-?" reflect current industry priorities. Innovative approaches utilizing biocatalysts and microwave-assisted synthesis have shown promise in reducing energy consumption and waste generation during its production. These advancements align with the pharmaceutical industry's push toward Process Intensification and Quality by Design (QbD) principles.

The analytical characterization of Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- employs advanced techniques such as HPLC-MS and NMR spectroscopy, addressing quality control concerns frequently searched by professionals ("How to analyze purity of CAS 898289-31-1?"). Its stability profile under various conditions has been extensively studied, with particular attention to storage recommendations (ambient temperature, desiccated environment) to maintain optimal performance in downstream applications.

From a commercial perspective, the global market for fine chemicals like Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- is expanding, driven by increased R&D investment in targeted therapies and personalized medicine. Supply chain professionals often search for "reliable suppliers of CAS 898289-31-1" and "technical specifications sheets", underscoring the need for comprehensive product documentation. The compound's classification under REACH compliance and other regulatory frameworks remains a critical consideration for international trade.

Future research directions for CAS 898289-31-1 include exploration of its potential in material science applications, particularly in the development of functional polymers and smart coatings. The compound's structural features suggest possible utility in creating molecularly imprinted polymers (MIPs) for sensor technologies - an area gaining traction in IoT and wearable devices. Such interdisciplinary applications answer emerging search queries like "Innovative uses of Benzaldehyde derivatives in materials".

For synthetic chemists, the regioselectivity and functional group compatibility of Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- make it particularly valuable in parallel synthesis and combinatorial chemistry approaches. Detailed reaction optimization studies have been published, addressing practical questions such as "Best catalysts for reactions with CAS 898289-31-1" and "Solvent effects on Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- reactivity". These resources are invaluable for process chemists working in API manufacturing.

In academic settings, CAS 898289-31-1 serves as an excellent case study for teaching advanced concepts in protective group chemistry and molecular design. Educational searches frequently include terms like "mechanism of THP protection in Benzaldehyde derivatives" and "spectral analysis of 2-substituted Benzaldehydes", highlighting its didactic value. The compound's balanced complexity makes it suitable for both undergraduate advanced labs and graduate-level research projects.

As the chemical industry continues to evolve toward more specialized intermediates, compounds like Benzaldehyde,2-[(tetrahydro-2H-pyran-4-yl)oxy]- will likely see increased utilization. Its combination of structural versatility and well-characterized properties positions it as a valuable tool for innovators across multiple scientific disciplines. Ongoing research will undoubtedly uncover new applications that leverage its unique chemical features in emerging technological fields.

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