• 1. An anti-biodegradable hydrophobic sulfonate-based acrylamide copolymer containing 2,4-dichlorophenoxy for enhanced oil recovery
  Shaohua Gou,Yang He,Lihua Zhou,Peng Zhao,Qin Zhang,Shiwei Li,Qipeng Guo New J. Chem. 2015 39 9265
• 2. A highly sensitive “ON–OFF” optical sensor for the selective detection of cyanide ions in 100% aqueous solutions based on hydrogen bonding and water assisted aggregation induced emission
  Ramo Nazarian,Hossein Reza Darabi,Kioumars Aghapoor,Rohoullah Firouzi,Hani Sayahi Chem. Commun. 2020 56 8992
• 3. Unexpected synthesis of indolo[1,2-c]quinazolines by a sequential Ugi 4CC–Staudinger–aza-Wittig–nucleophilic addition reaction
  Ping He,Yi-Bo Nie,Jing Wu,Ming-Wu Ding Org. Biomol. Chem. 2011 9 1429
• 4. Unexpected synthesis of indolo[1,2-c]quinazolines by a sequential Ugi 4CC–Staudinger–aza-Wittig–nucleophilic addition reaction
  Ping He,Yi-Bo Nie,Jing Wu,Ming-Wu Ding Org. Biomol. Chem. 2011 9 1429
• 5. Synthesis of α,α-disubstituted acetic acids using low-valent titanium
  Mariano García,Carmen del Campo,Emilio F. Llama,José V. Sinisterra J. Chem. Soc. Perkin Trans. 1 1995 1771

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Chlorobenzenes
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Halobenzenes Chlorobenzenes

Comprehensive Guide to 2-(2,4-Dichlorophenoxy)acetamide (CAS No. 1982-42-9): Properties, Applications, and Market Insights

2-(2,4-Dichlorophenoxy)acetamide (CAS No. 1982-42-9) is a specialized organic compound with significant applications in agricultural and industrial sectors. This chemical, often referred to as 2,4-D acetamide, is a derivative of phenoxyacetic acid and is widely recognized for its role in plant growth regulation and herbicide formulations. Its unique molecular structure, featuring two chlorine atoms and an acetamide group, contributes to its distinct chemical properties and functional versatility.

The compound's chemical formula C8H7Cl2NO2 and molecular weight of 220.05 g/mol make it a moderately stable substance under standard conditions. Researchers and industry professionals frequently search for "2-(2,4-Dichlorophenoxy)acetamide uses" or "CAS 1982-42-9 properties" to understand its behavior in various environments. The substance typically appears as a white to off-white crystalline powder with a melting point range of 150-155°C, making it suitable for formulation in different agricultural products.

In modern agriculture, 2-(2,4-Dichlorophenoxy)acetamide plays a crucial role in selective weed control systems. Farmers and agronomists often inquire about "2,4-D acetamide herbicide formulations" as it demonstrates effective action against broadleaf weeds while being relatively safe for grass crops. The compound's mode of action involves mimicking natural plant hormones, disrupting normal growth patterns in target species. Recent studies have explored its potential in combination with other active ingredients to enhance efficacy and reduce environmental impact.

The industrial applications of CAS 1982-42-9 extend beyond agriculture. Chemical manufacturers frequently investigate "2-(2,4-Dichlorophenoxy)acetamide synthesis" for developing specialized intermediates in pharmaceutical and specialty chemical production. Its reactive acetamide group makes it valuable for creating more complex molecules through various chemical transformations. The compound's stability and predictable reactivity profile contribute to its popularity in research and development laboratories.

Environmental considerations surrounding 2,4-D acetamide have become a significant topic of discussion among regulatory bodies and environmental scientists. Searches for "2-(2,4-Dichlorophenoxy)acetamide environmental fate" and "CAS 1982-42-9 biodegradation" reflect growing interest in understanding its persistence and breakdown products in ecosystems. Recent advancements in analytical chemistry have enabled more precise monitoring of its environmental behavior, leading to improved application guidelines and safety protocols.

The global market for 2-(2,4-Dichlorophenoxy)acetamide has shown steady growth, particularly in regions with intensive agricultural production. Industry analysts often track "2,4-D acetamide market trends" to understand supply-demand dynamics and pricing fluctuations. The compound's position in the agrochemical sector remains strong, though innovations in formulation technology and application methods continue to shape its commercial landscape. Manufacturers are increasingly focusing on developing more efficient and environmentally friendly delivery systems for this active ingredient.

Quality control and analytical methods for CAS 1982-42-9 have evolved significantly with technological advancements. Laboratories frequently search for "2-(2,4-Dichlorophenoxy)acetamide HPLC methods" or "spectroscopic analysis of 2,4-D acetamide" to ensure product purity and consistency. Modern chromatographic techniques, particularly reverse-phase HPLC with UV detection, have become standard for quantifying the compound in various matrices, from technical-grade materials to formulated products.

Safety considerations for handling 2,4-D acetamide remain an important aspect of its industrial and agricultural use. While not classified as highly hazardous, proper personal protective equipment (PPE) and handling procedures are recommended. Researchers often look for "2-(2,4-Dichlorophenoxy)acetamide safety data" to ensure compliance with workplace safety regulations. The compound's material safety data sheet (MSDS) provides comprehensive information about storage conditions, incompatibilities, and first-aid measures.

Future research directions for 2-(2,4-Dichlorophenoxy)acetamide include exploring its potential in novel applications beyond traditional uses. Scientific inquiries about "2,4-D acetamide derivatives" and "CAS 1982-42-9 structure-activity relationships" indicate growing interest in modifying its molecular structure to enhance specific properties or create new functionalities. These investigations may lead to breakthroughs in various fields, from crop protection to materials science.

In conclusion, 2-(2,4-Dichlorophenoxy)acetamide (CAS No. 1982-42-9) represents an important chemical entity with diverse applications and ongoing research potential. Its established role in agriculture, combined with emerging opportunities in other sectors, ensures continued relevance in scientific and industrial communities. As understanding of its properties and effects deepens, and as formulation technologies advance, this compound is likely to maintain its position as a valuable tool in chemical applications while adapting to evolving environmental and regulatory requirements.

• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)