• 1. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?
  Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
• 2. Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices
  Dhirendra K. Chaudhary,Pramendra Kumar,Lokendra Kumar RSC Adv., 2016,6, 94731-94738
• 3. Fast synthesis of copper nanoclusters through the use of hydrogen peroxide additive and their application for the fluorescence detection of Hg2+ in water samples?
  Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
• 4. Evolution of hierarchical porous structures in supramolecular guest–host hydrogels?
  Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
• 5. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693

• Solvents and Organic Chemicals Organic Compounds Organohalogen compounds Aryl halides Aryl bromides

Comprehensive Guide to (4-Bromothiophen-3-yl)methanol (CAS No. 70260-05-8): Properties, Applications, and Market Insights

(4-Bromothiophen-3-yl)methanol (CAS No. 70260-05-8) is a specialized brominated thiophene derivative with significant relevance in pharmaceutical and material science research. This compound, characterized by its thiophene ring substituted with a bromine atom and a hydroxymethyl group, serves as a versatile building block in organic synthesis. Its molecular formula, C₅H₅BrOS, and molecular weight of 193.06 g/mol make it a valuable intermediate for designing complex molecules.

The growing interest in heterocyclic compounds like (4-Bromothiophen-3-yl)methanol stems from their applications in drug discovery and functional materials. Researchers frequently search for "bromothiophene derivatives uses" or "thiophene-based intermediates," reflecting its importance in developing antiviral agents and organic semiconductors. Recent studies highlight its role in synthesizing kinase inhibitors, a hot topic in cancer research, aligning with trends in personalized medicine.

From a chemical perspective, (4-Bromothiophen-3-yl)methanol exhibits unique reactivity due to its electron-rich thiophene core and bromine substituent. The hydroxymethyl group allows for further functionalization through esterification or oxidation, making it pivotal for creating conjugated polymers—a key area in OLED technology development. Industry searches for "thiophene methanol synthesis" or "brominated heterocycle applications" underscore its commercial relevance.

In material science, this compound contributes to advancements in organic electronics, particularly in flexible displays and solar cells. Its incorporation into π-conjugated systems enhances charge transport properties, addressing the global demand for sustainable energy solutions. The rise in queries about "green chemistry thiophenes" mirrors the compound's alignment with eco-friendly synthesis initiatives.

The market for (4-Bromothiophen-3-yl)methanol shows steady growth, driven by pharmaceutical R&D and electronic material innovations. Suppliers often catalog it under high-purity chemical intermediates, with quality specifications emphasizing ≥98% purity for research applications. Analytical techniques like HPLC and NMR are crucial for verifying its structural integrity, as noted in frequent searches for "CAS 70260-05-8 characterization."

Storage and handling recommendations for (4-Bromothiophen-3-yl)methanol include protection from light and moisture at 2-8°C, following standard practices for air-sensitive organics. While not classified as hazardous under normal conditions, proper laboratory safety protocols should always be observed—a point emphasized in guidelines searched as "safe handling of bromoaromatics."

Future research directions may explore its potential in bioconjugation chemistry or as a precursor for metal-organic frameworks (MOFs), areas gaining traction in nanotechnology circles. The compound's adaptability positions it well to address emerging challenges in medicinal chemistry and smart materials, ensuring continued scientific and industrial interest.

• 1501857-92-6(2-(4-Bromothiophen-3-yl)propan-2-ol)
• 73919-89-8((4,5-Dibromothiophen-3-yl)methanol)
• 2432848-81-0(3-Bromo-4-(methoxymethyl)thiophene)
• 30318-99-1(3-Bromo-4-methylthiophene)
• 2952896-37-4(2-(4-bromothiophen-3-yl-2,5-d2)propan-1,1,1,3,3,3-d6-2-ol)
• 614730-07-3(THIOPHENE, 3-BROMO-4-(DIMETHOXYMETHYL)-)
• 16694-17-0(4-Bromothiophene-3-carboxylic acid)
• 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)