• 1. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
  Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
• 2. Evidence that the availability of an allylic hydrogen governs the regioselectivity of the Wacker oxidation
  Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
• 3. Exchanged ligands on the surface of a giant cluster: [(MoO3)176(H2O)63(CH3OH)17Hn](32 – n)–
  Chem. Commun., 1998, 1501-1502
• 4. Excimer and exciplex formation in a pair of bright phosphorescent isomers constructed from Cu3(pyrazolate)3 and Cu3I3 coordination luminophores?
  Shun-Ze Zhan,Mian Li,Xiao-Ping Zhou,Dan Li,Seik Weng Ng RSC Adv., 2011,1, 1457-1459
• 5. Exciting clusters, what does off-resonance actually mean??
  Goonay Yousefalizadeh,Shideh Ahmadi,Nicholas J. Mosey,Kevin G. Stamplecoskie Nanoscale, 2021,13, 242-252

• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid esters
• Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid derivatives Carboxylic acid esters

Comprehensive Overview of 1,2-Dichloroethanol Acetate (CAS No. 10140-87-1): Properties, Applications, and Industry Insights

1,2-Dichloroethanol Acetate (CAS No. 10140-87-1) is a specialized organic compound with a unique molecular structure, combining chloro and acetate functional groups. This chemical has garnered attention in industrial and research settings due to its versatile reactivity and role as an intermediate in synthetic processes. In this article, we delve into its physical and chemical properties, synthesis methods, and applications, while addressing trending topics such as sustainable chemistry and green alternatives in modern manufacturing.

The compound's systematic name, 1,2-Dichloroethyl acetate, reflects its molecular composition, where two chlorine atoms are bonded to adjacent carbon atoms, and an acetate group completes the ester functionality. Its CAS registry number, 10140-87-1, serves as a universal identifier for precise classification in chemical databases. Researchers often search for "1,2-Dichloroethanol Acetate solubility" or "10140-87-1 safety data," highlighting the need for accurate technical information. The compound's boiling point, density, and refractive index are critical parameters for laboratory and industrial use.

In recent years, the demand for eco-friendly solvents and bio-based intermediates has surged, prompting investigations into compounds like 1,2-Dichloroethanol Acetate. While it is not a direct replacement for conventional solvents, its selective reactivity makes it valuable in controlled applications. For instance, it serves as a precursor in the synthesis of pharmaceutical intermediates and specialty polymers, where precise molecular design is paramount. Searches for "biodegradable chemical alternatives" and "low-toxicity esters" align with discussions about this compound's niche utility.

From a technical perspective, 1,2-Dichloroethanol Acetate exhibits moderate polarity, making it soluble in common organic solvents like ethanol and diethyl ether. Its stability under ambient conditions is a frequently queried topic, with users seeking "storage recommendations for 10140-87-1." Proper handling involves inert atmospheres and moisture-free environments to prevent hydrolysis. Analytical techniques such as GC-MS and NMR spectroscopy are typically employed to verify its purity, a key concern for high-precision applications.

The compound's role in material science is another area of interest. For example, it has been explored as a modifier in polymer blends to enhance thermal stability. Queries like "1,2-Dichloroethanol Acetate in polymer synthesis" reflect this application. Additionally, its potential in agrochemical formulations has been studied, though regulatory compliance remains a critical consideration. Industry professionals often search for "CAS 10140-87-1 regulatory status" to ensure adherence to regional guidelines.

Innovations in catalytic processes have further expanded the utility of 1,2-Dichloroethanol Acetate. Recent studies focus on optimizing its production via catalytic esterification, reducing energy consumption and byproduct formation. These advancements resonate with global trends toward energy-efficient chemistry, a hot topic in academic and industrial forums. Users frequently inquire about "scalable synthesis of 1,2-Dichloroethyl acetate" or "cost-effective production methods," underscoring the need for practical solutions.

In conclusion, 1,2-Dichloroethanol Acetate (CAS No. 10140-87-1) represents a multifaceted compound with applications spanning pharmaceuticals, materials, and specialty chemicals. Its relevance persists amid evolving industry demands for sustainability and efficiency. By addressing common search queries and integrating contemporary themes like green chemistry, this overview aims to bridge technical expertise with real-world relevance, offering a resource for researchers and professionals alike.

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• 148440-72-6(Carbonochloridic acid, 1,2,2,2-tetrachloroethyl ester, (±)-)
• 43084-23-7(Ethane, 1,2-dichloro-1,2-dimethoxy-, (R*,S*)-)
• 412026-17-6(2-Oxepanone, 7-chloro-)
• 195968-31-1(Ethanol, 2-[2-(1-chloroethoxy)ethoxy]-, acetate)
• 339984-86-0(Propane, 1-(1,2-dichloroethoxy)-)
• 352320-86-6(Acetic acid, chloro[(chlorocarbonyl)oxy]-, ethyl ester)
• 352320-88-8(Acetic acid, chloro[(chlorocarbonyl)oxy]-, 1-methylethyl ester)
• 352320-90-2(Acetic acid, chloro[(chlorocarbonyl)oxy]-, butyl ester)
• 15175-05-0(Undecanoic acid, 2-chloroethyl ester)