• 1. Evidence of CO2 molecule acting as an electron acceptor on a nanoporous metal–organic-framework MIL-53 or Cr3+(OH)(O2C–C6H4–CO2)?
  Alexandre Vimont,Arnaud Travert,Philippe Bazin,Jean-Claude Lavalley,Marco Daturi,Christian Serre,Gérard Férey,Sandrine Bourrelly,Philip L. Llewellyn Chem. Commun., 2007, 3291-3293
• 2. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
  Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
• 3. Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction?
  Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
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• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Carbonyl compounds Aldehydes

Comprehensive Guide to 3,4-Dichloro-2-hydroxybenzaldehyde (CAS No. 23602-61-1): Properties, Applications, and Industry Insights

3,4-Dichloro-2-hydroxybenzaldehyde (CAS No. 23602-61-1) is a specialized organic compound widely recognized for its unique chemical structure and versatile applications. This aromatic aldehyde features a hydroxyl group and two chlorine atoms attached to a benzene ring, making it a valuable intermediate in synthetic chemistry. Its molecular formula, C7H4Cl2O2, and distinct properties have garnered attention across pharmaceuticals, agrochemicals, and material science industries.

In recent years, the demand for halogenated benzaldehydes like 3,4-Dichloro-2-hydroxybenzaldehyde has surged due to their role in developing high-performance materials and bioactive molecules. Researchers frequently search for "synthesis of 3,4-Dichloro-2-hydroxybenzaldehyde" or "CAS 23602-61-1 applications," reflecting its growing relevance. The compound’s ability to act as a precursor for antimicrobial agents and UV stabilizers aligns with global trends toward sustainable and functional chemicals.

The physicochemical properties of 3,4-Dichloro-2-hydroxybenzaldehyde include a melting point range of 120–125°C and moderate solubility in polar organic solvents. These characteristics make it suitable for controlled reactions in fine chemical synthesis. Industry professionals often inquire about "safety data for CAS 23602-61-1" or "suppliers of halogenated benzaldehydes," emphasizing the need for reliable sourcing and handling protocols.

From an environmental perspective, the compound’s biodegradability and eco-friendly derivatives are under investigation. Queries like "green chemistry alternatives to 3,4-Dichloro-2-hydroxybenzaldehyde" highlight the shift toward sustainable practices. Innovations in catalytic oxidation and microwave-assisted synthesis have further optimized its production, reducing energy consumption and waste generation.

In pharmaceuticals, 3,4-Dichloro-2-hydroxybenzaldehyde serves as a building block for heterocyclic compounds with potential therapeutic effects. Its derivatives are explored for anti-inflammatory and antioxidant properties, resonating with the health-conscious consumer trend. Analytical techniques such as HPLC and NMR are critical for quality control, as purity directly impacts downstream applications.

The compound’s role in agrochemical formulations is another area of interest. Farmers and researchers seek "3,4-Dichloro-2-hydroxybenzaldehyde in crop protection" due to its utility in designing herbicides and fungicides. Regulatory compliance, including REACH and EPA guidelines, ensures its safe use in these applications.

Emerging technologies like AI-driven molecular design are accelerating the discovery of new applications for CAS 23602-61-1. Computational models predict its reactivity, reducing trial-and-error in labs. Meanwhile, market analyses project steady growth for halogenated aromatic aldehydes, driven by R&D investments in Asia-Pacific and North America.

To summarize, 3,4-Dichloro-2-hydroxybenzaldehyde exemplifies the intersection of innovation and practicality in modern chemistry. Its multifaceted uses, from drug development to material engineering, underscore its importance. As industries prioritize efficiency and sustainability, this compound will remain a focal point for scientific and commercial advancements.

• 27164-09-6(3,6-dichloro-2-hydroxybenzaldehyde)
• 32596-43-3(5-Chloro-2-hydroxyisophthalaldehyde)
• 49860-79-9(Cobalt,bis(3,5-dichloro-2-hydroxybenzaldehydato-O,O')- (9CI))
• 23602-63-3(5-Chloro-2-hydroxy-3-methylbenzaldehyde)
• 635-93-8(5-Chlorosalicylaldehyde)
• 1927-94-2(3-Chloro-2-hydroxybenzaldehyde)
• 832097-02-6(Benzaldehyde, 3-chloro-2-hydroxy-5-(hydroxymethyl)-)
• 2420-26-0(4-Chloro-2-hydroxybenzaldehyde)
• 90-60-8(3,5-Dichlorosalicylaldehyde)
• 73275-97-5(Benzaldehyde,4,5-dichloro-2,3-dihydroxy-)