• 1. Cascade enzymatic cleavage of the β-O-4 linkage in a lignin model compound
  Elena Rosini,Chiara Allegretti,Roberta Melis,Lorenzo Cerioli,Gianluca Conti,Loredano Pollegioni,Paola D'Arrigo Catal. Sci. Technol. 2016 6 2195
• 2. Catalyst choice impacts aromatic monomer yields and selectivity in hydrogen-free reductive catalytic fractionation
  Jacob K. Kenny,David G. Brandner,Sasha R. Neefe,William E. Michener,Yuriy Román-Leshkov,Gregg T. Beckham,J. Will Medlin React. Chem. Eng. 2022 7 2527
• 3. Syntheses of 2-methoxyestradiol and eugenol template based diarylpropenes as non-steroidal anticancer agents
  Vinay Pathak,Imran Ahmad,Amandeep Kaur Kahlon,Mohammad Hasanain,Sandeep Sharma,Kishore K. Srivastava,Jayanta Sarkar,Karuna Shankar,Ashok Sharma,Atul Gupta RSC Adv. 2014 4 35171
• 4. Enzymatic cleavage of lignin β-O-4 aryl ether bonds via net internal hydrogen transfer
  Jochen Reiter,Harald Strittmatter,Lars O. Wiemann,Doris Schieder,Volker Sieber Green Chem. 2013 15 1373
• 5. Analysis of gas chromatography/mass spectrometry data for catalytic lignin depolymerization using positive matrix factorization
  Yu Gao,Michael J. Walker,Jacob A. Barrett,Omid Hosseinaei,David P. Harper,Peter C. Ford,Brent J. Williams,Marcus B. Foston Green Chem. 2018 20 4366

• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Alkyl-phenylketones

Comprehensive Overview of 1-(4-Hydroxy-3-methoxyphenyl)-1-propanone (CAS No. 1835-14-9)

1-(4-Hydroxy-3-methoxyphenyl)-1-propanone, with the CAS number 1835-14-9, is an organic compound widely recognized for its role in flavor and fragrance applications. This compound, also referred to as 4-hydroxy-3-methoxypropiophenone, belongs to the class of aromatic ketones and exhibits unique chemical properties that make it valuable in various industries. Its molecular structure features a propanone backbone attached to a hydroxy-methoxyphenyl group, contributing to its distinct characteristics.

In recent years, the demand for natural and synthetic flavoring agents has surged, driven by consumer preferences for enhanced sensory experiences in food and beverages. 1-(4-Hydroxy-3-methoxyphenyl)-1-propanone is often explored for its potential as a vanillin precursor, a compound highly sought after in the food industry. Researchers and manufacturers are increasingly focusing on sustainable production methods, aligning with the global trend toward green chemistry and eco-friendly processes.

The compound's CAS No. 1835-14-9 is frequently searched in academic and industrial databases, reflecting its relevance in organic synthesis and pharmaceutical intermediates. Its applications extend to the development of cosmetic ingredients, where its aromatic properties are leveraged to create appealing fragrances. Additionally, its potential antioxidant properties have sparked interest in the health and wellness sector, particularly in the formulation of nutraceuticals.

From a technical perspective, 1-(4-Hydroxy-3-methoxyphenyl)-1-propanone is characterized by its melting point, solubility, and stability under various conditions. These properties are critical for its integration into industrial processes. For instance, its solubility in organic solvents like ethanol and acetone makes it a versatile component in laboratory and manufacturing settings. Analytical techniques such as HPLC and GC-MS are commonly employed to assess its purity and quality.

The growing interest in bioactive compounds has further elevated the significance of CAS 1835-14-9. Studies investigating its potential anti-inflammatory and neuroprotective effects have been published in peer-reviewed journals, attracting attention from the scientific community. This aligns with the broader trend of exploring plant-derived metabolites for therapeutic applications, a topic frequently searched in AI-driven research platforms.

In the context of market trends, the compound's supply chain and global availability are subjects of interest for procurement specialists. With the rise of e-commerce platforms for chemical sourcing, queries related to bulk purchasing and technical specifications of 1-(4-Hydroxy-3-methoxyphenyl)-1-propanone have increased. Suppliers often highlight its compliance with international safety standards, ensuring its suitability for diverse applications.

Looking ahead, the versatility of 1-(4-Hydroxy-3-methoxyphenyl)-1-propanone positions it as a compound of enduring relevance. Whether in flavor enhancement, fragrance formulation, or biomedical research, its multifaceted applications continue to drive innovation. As industries evolve toward sustainable and efficient solutions, this compound is poised to play a pivotal role in meeting future demands.

• 5438-67-5(1,2-bis(4-hydroxy-3-methoxyphenyl)ethanone)
• 1835-04-7(3,4-Dimethoxypropiophenone)
• 5658-50-4(1-(3,4,5-trimethoxyphenyl)propan-1-one)
• 3141-93-3(Benzyl 3,4-dimethoxyphenyl ketone)
• 5650-43-1(1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one)
• 4927-55-3(1,2-bis(3,4-dimethoxyphenyl)-ethanone)
• 87282-25-5(Ethanone, 2-phenyl-1-(3,4,5-trimethoxyphenyl)-)
• 29955-23-5(Ethanone, 2-(3,4-dimethoxyphenyl)-1-phenyl-)
• 63661-66-5(1-Propanone, 1-(4-hydroxy-3-methoxyphenyl)-, sodium salt)
• 58451-99-3(Ethanone, 1-(3-hydroxy-4-methoxyphenyl)-2-phenyl-)