Cas no 10522-23-3 (2-(naphthalen-2-yl)propanal)

2-(naphthalen-2-yl)propanal structure
2-(naphthalen-2-yl)propanal structure
Product Name:2-(naphthalen-2-yl)propanal
CAS No:10522-23-3
MF:C13H12O
MW:184.233783721924
CID:1151637
PubChem ID:10856176
Update Time:2025-11-01

2-(naphthalen-2-yl)propanal Chemical and Physical Properties

Names and Identifiers

    • 2-Naphthaleneacetaldehyde, a-methyl-
    • 2-(naphthalen-2-yl)propanal
    • 10522-23-3
    • 2-(2-naphthyl) propanal
    • F1967-2637
    • Z1268606413
    • AKOS015258386
    • 2-naphthalen-2-ylpropanal
    • EN300-1225193
    • SCHEMBL1663207
    • Inchi: 1S/C13H12O/c1-10(9-14)12-7-6-11-4-2-3-5-13(11)8-12/h2-10H,1H3
    • InChI Key: MJNMZHAZYDYGMQ-UHFFFAOYSA-N
    • SMILES: O=CC(C)C1C=CC2C=CC=CC=2C=1

Computed Properties

  • Exact Mass: 184.08886
  • Monoisotopic Mass: 184.088815002g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 199
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.5
  • Topological Polar Surface Area: 17.1?2

Experimental Properties

  • PSA: 17.07

2-(naphthalen-2-yl)propanal Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
N756650-10mg
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$ 50.00 2022-06-03
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$ 210.00 2022-06-03
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Additional information on 2-(naphthalen-2-yl)propanal

Exploring the Versatile Applications and Properties of 2-Naphthaleneacetaldehyde, a-methyl- (CAS No. 10522-23-3)

2-Naphthaleneacetaldehyde, a-methyl- (CAS No. 10522-23-3) is a specialized organic compound that has garnered significant attention in the fragrance, flavor, and pharmaceutical industries. This aromatic aldehyde, with its unique molecular structure, offers a wide range of applications, making it a valuable ingredient in various formulations. Its chemical properties and synthetic versatility have positioned it as a key component in research and industrial processes.

The compound is characterized by its naphthalene backbone and an acetaldehyde functional group with a methyl substitution. This structural configuration imparts distinct aromatic qualities, which are highly sought after in the creation of perfumes and flavors. The CAS No. 10522-23-3 is often referenced in scientific literature and industry databases, highlighting its importance in organic chemistry.

One of the most notable applications of 2-Naphthaleneacetaldehyde, a-methyl- is in the fragrance industry. Its rich, woody aroma with subtle floral undertones makes it a popular choice for high-end perfumes and colognes. Perfumers value this compound for its ability to enhance the depth and longevity of scents, contributing to the creation of complex and enduring fragrance profiles.

In the flavor industry, this compound is used to impart unique aromatic notes to food and beverage products. Its ability to blend seamlessly with other flavoring agents allows for the development of sophisticated taste profiles. The increasing demand for natural and synthetic flavor enhancers has further driven the interest in CAS No. 10522-23-3 as a versatile ingredient.

Beyond its sensory applications, 2-Naphthaleneacetaldehyde, a-methyl- plays a crucial role in pharmaceutical research. Its molecular structure serves as a building block for the synthesis of various bioactive compounds. Researchers are exploring its potential in developing new therapeutic agents, particularly in the fields of anti-inflammatory and antimicrobial treatments. The compound's ability to interact with biological systems makes it a promising candidate for future drug development.

The synthetic pathways for producing 2-Naphthaleneacetaldehyde, a-methyl- have been extensively studied, with advancements in green chemistry leading to more sustainable production methods. Innovations in catalytic processes and solvent-free reactions have reduced the environmental impact of its synthesis, aligning with the growing emphasis on eco-friendly chemical manufacturing.

Market trends indicate a steady rise in the demand for CAS No. 10522-23-3, driven by its diverse applications and the expanding fragrance and flavor industries. The compound's stability and compatibility with other ingredients make it a preferred choice for formulators seeking reliable and high-performance additives. As consumer preferences evolve towards more complex and unique sensory experiences, the relevance of 2-Naphthaleneacetaldehyde, a-methyl- is expected to grow.

In conclusion, 2-Naphthaleneacetaldehyde, a-methyl- (CAS No. 10522-23-3) stands out as a multifaceted compound with significant industrial and research value. Its applications in fragrances, flavors, and pharmaceuticals underscore its versatility, while ongoing advancements in synthesis methods ensure its sustainable production. As industries continue to innovate, this compound will undoubtedly remain a key player in the realm of organic chemistry.

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