Cas no 221195-30-8 (Benzenenonanal)

Benzenenonanal structure
Benzenenonanal structure
Product Name:Benzenenonanal
CAS No:221195-30-8
MF:C15H22O
MW:218.334584712982
CID:1407979
PubChem ID:19601718
Update Time:2025-10-18

Benzenenonanal Chemical and Physical Properties

Names and Identifiers

    • Benzenenonanal
    • 221195-30-8
    • 9-phenylnonanal
    • SCHEMBL6577467
    • 9-Phenyl-1-nonanone
    • 9-(phenyl)-nonan-1-al
    • Inchi: 1S/C15H22O/c16-14-10-5-3-1-2-4-7-11-15-12-8-6-9-13-15/h6,8-9,12-14H,1-5,7,10-11H2
    • InChI Key: WSASXIBTVWLWKR-UHFFFAOYSA-N
    • SMILES: O=CCCCCCCCCC1C=CC=CC=1

Computed Properties

  • Exact Mass: 218.16716
  • Monoisotopic Mass: 218.167
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 9
  • Complexity: 159
  • 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: 4.6
  • Topological Polar Surface Area: 17.1A^2

Experimental Properties

  • PSA: 17.07

Benzenenonanal Security Information

Benzenenonanal Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
B537333-10mg
Benzenenonanal
221195-30-8
10mg
$ 50.00 2022-06-07
TRC
B537333-50mg
Benzenenonanal
221195-30-8
50mg
$ 135.00 2022-06-07
TRC
B537333-100mg
Benzenenonanal
221195-30-8
100mg
$ 230.00 2022-06-07

Benzenenonanal Related Literature

Additional information on Benzenenonanal

Benzenenonanal (CAS No. 221195-30-8): A Comprehensive Overview in Modern Chemical Research

Benzenenonanal, identified by the Chemical Abstracts Service Number (CAS No.) 221195-30-8, is a significant compound in the realm of organic chemistry and pharmaceutical research. This aldehyde derivative of benzene exhibits unique structural and functional properties that make it a subject of intense interest among scientists. The compound's molecular structure, characterized by a benzene ring substituted with a nonanal aldehyde group, positions it as a valuable intermediate in synthetic chemistry and a potential candidate for various biological applications.

The chemical formula of Benzenenonanal is C14H14O, reflecting its composition of carbon, hydrogen, and oxygen atoms. The presence of the aldehyde functional group (–CHO) at the end of the nonanal side chain contributes to its reactivity, making it a versatile building block for more complex molecules. This reactivity has been leveraged in the development of novel synthetic pathways and in the synthesis of bioactive compounds.

In recent years, Benzenenonanal has garnered attention for its potential applications in pharmaceuticals. Aldehydes, in general, are known for their role as intermediates in the synthesis of various drugs and natural products. The specific properties of Benzenenonanal, such as its aromaticity and the length of its aldehyde chain, make it particularly useful in the construction of complex organic molecules. Researchers have been exploring its utility in the development of new therapeutic agents, including those targeting neurological disorders and inflammatory conditions.

One of the most promising areas of research involving Benzenenonanal is its application as a precursor in the synthesis of pharmacologically active compounds. For instance, studies have demonstrated its role in the preparation of nonsteroidal anti-inflammatory drug (NSAID) analogs. These NSAIDs are widely used for their pain-relieving and anti-inflammatory effects, and the development of new derivatives is an ongoing effort in medicinal chemistry. The ability to incorporate Benzenenonanal into these structures allows for fine-tuning of biological activity and improved pharmacokinetic profiles.

The structural flexibility offered by Benzenenonanal also makes it a valuable tool in material science. Researchers have investigated its potential use in the development of polymers and coatings that exhibit enhanced durability and functionality. The aldehyde group can participate in various chemical reactions, such as condensation reactions with amino acids or other aldehydes, leading to the formation of cross-linked networks. These networks can impart desirable properties to materials, such as increased thermal stability or improved mechanical strength.

In addition to its synthetic applications, Benzenenonanal has been studied for its potential role in sensory biology. Aldehydes are known to interact with olfactory receptors, contributing to their characteristic smells. The unique aroma profile of Benzenenonanal has been explored by researchers interested in natural product chemistry and flavor science. By understanding how this compound interacts with sensory systems, scientists can gain insights into broader questions about olfaction and chemical communication.

The latest research on Benzenenonanal also highlights its significance in environmental chemistry. Studies have examined its degradation pathways and interactions with biological systems under various environmental conditions. Understanding these processes is crucial for assessing the environmental impact of chemical compounds and for developing strategies to minimize their negative effects. The findings from these studies contribute to a more comprehensive understanding of how organic compounds behave in natural ecosystems.

The synthesis and characterization of Benzenenonanal have been facilitated by advancements in analytical techniques such as nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry (MS), and X-ray crystallography. These tools have enabled researchers to determine the precise structure and conformational preferences of the compound, providing critical data for further studies. The high-resolution structural information obtained from these techniques has been instrumental in guiding synthetic modifications and optimizing reaction conditions.

In conclusion, Benzenennaanaa, with CAS No.221195-30-8, represents a fascinating compound with diverse applications across multiple scientific disciplines. Its unique chemical properties make it a valuable tool in pharmaceutical research, material science, sensory biology, and environmental chemistry. As research continues to uncover new aspects of this compound's behavior and potential uses, it is likely to remain a cornerstone molecule in modern chemical investigations.

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