• 1. Enabling stable MnO2 matrix for aqueous zinc-ion battery cathodes?
  Yiding Jiao,Liqun Kang,Jasper Berry-Gair,Kit McColl,Jianwei Li,Haobo Dong,Hao Jiang,Ryan Wang,Furio Corà,Dan J. L. Brett,Ivan P. Parkin J. Mater. Chem. A, 2020,8, 22075-22082
• 2. Ester-directed orthogonal dual C–H activation and ortho aryl C–H alkenylation via distal weak coordination?
  Manickam Bakthadoss,Tadiparthi Thirupathi Reddy,Vishal Agarwal,Duddu S. Sharada Chem. Commun., 2022,58, 1406-1409
• 3. Evolutionary approaches in protein engineering towards biomaterial construction
  Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
• 4. Distinct correlation between (CN2)x units and pores: a low-cost method for predesigned wide range control of micropore size of porous carbon?
  Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966
• 5. Emulsion technologies for multicellular tumour spheroid radiation assays?
  Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110

• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Phenol ethers
• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers

3-(Benzyloxy)-5-hydroxybenzyl Alcohol (CAS No. 134868-93-2): A Comprehensive Guide to Its Properties and Applications

3-(Benzyloxy)-5-hydroxybenzyl Alcohol (CAS No. 134868-93-2) is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, cosmetics, and material science. This compound, characterized by its unique benzyl-protected hydroxyl group and aromatic alcohol structure, serves as a versatile intermediate in synthetic chemistry. Researchers and industry professionals often search for terms like "3-(Benzyloxy)-5-hydroxybenzyl Alcohol synthesis" or "CAS 134868-93-2 applications," highlighting its growing relevance in modern science.

The molecular structure of 3-(Benzyloxy)-5-hydroxybenzyl Alcohol features a benzyl ether group attached to a phenolic ring, which is further substituted with a hydroxymethyl moiety. This arrangement provides the compound with unique reactivity, making it valuable for organic synthesis and drug development. Recent trends in sustainable chemistry have also sparked interest in its potential as a green chemistry intermediate, aligning with the global push for eco-friendly manufacturing processes.

In the pharmaceutical industry, 3-(Benzyloxy)-5-hydroxybenzyl Alcohol is frequently explored as a building block for active pharmaceutical ingredients (APIs). Its ability to undergo selective deprotection and functionalization makes it a preferred choice for designing targeted drug molecules. Searches for "benzyl-protected alcohol in drug synthesis" or "CAS 134868-93-2 in medicinal chemistry" reflect the compound's importance in this domain.

Beyond pharmaceuticals, this compound finds applications in cosmetic formulations, particularly in the development of antioxidant and anti-aging products. The phenolic hydroxyl group contributes to its potential radical-scavenging properties, a feature highly sought after in skincare research. This aligns with current consumer trends favoring science-backed cosmetic ingredients and natural-derived actives.

From a technical perspective, the physical and chemical properties of 3-(Benzyloxy)-5-hydroxybenzyl Alcohol make it suitable for various industrial applications. Its moderate solubility in organic solvents and stability under standard conditions facilitate its use in laboratory settings and scale-up processes. Analytical techniques such as HPLC, NMR, and mass spectrometry are commonly employed to characterize this compound, as evidenced by frequent searches for "CAS 134868-93-2 analytical methods."

The synthesis of 3-(Benzyloxy)-5-hydroxybenzyl Alcohol typically involves selective protection of phenolic groups followed by controlled reduction steps. Recent advancements in catalytic methods have improved the efficiency of its production, addressing growing demands from the fine chemical industry. These developments respond to market needs for cost-effective synthetic routes and high-purity intermediates.

Quality control remains paramount when working with 3-(Benzyloxy)-5-hydroxybenzyl Alcohol, particularly for GMP applications. Stringent specification requirements ensure its suitability for sensitive formulations, a topic frequently searched as "CAS 134868-93-2 purity standards." The compound's stability profile and storage considerations are also critical aspects for end-users across various industries.

Emerging research directions for 3-(Benzyloxy)-5-hydroxybenzyl Alcohol include its potential in material science applications, particularly as a precursor for functional polymers and specialty coatings. The compound's aromatic structure offers opportunities for creating advanced materials with tailored properties, meeting the increasing demand for high-performance chemicals in technological applications.

For researchers investigating structure-activity relationships, 3-(Benzyloxy)-5-hydroxybenzyl Alcohol provides an interesting case study in molecular modification strategies. Its well-defined chemical behavior makes it valuable for mechanistic studies and method development in organic chemistry. These academic applications contribute to its ongoing relevance in scientific literature and research publications.

As regulatory landscapes evolve, proper documentation and safety assessments for 3-(Benzyloxy)-5-hydroxybenzyl Alcohol remain essential. While not classified as hazardous under standard conditions, appropriate handling procedures should be followed, as with all laboratory chemicals. This practical consideration addresses common queries about "CAS 134868-93-2 safety data" and "benzyl alcohol derivatives handling."

The commercial availability of 3-(Benzyloxy)-5-hydroxybenzyl Alcohol from multiple chemical suppliers ensures accessibility for diverse applications. Market trends indicate growing demand for this compound, particularly from contract research organizations and specialty chemical manufacturers. This commercial aspect complements its scientific significance, creating a robust ecosystem around this valuable chemical entity.

• 3769-42-4(1,3-Dibenzyloxybenzene)
• 621-91-0(1,4-Dibenzyloxybenzene)
• 6214-44-4(4-Ethoxybenzyl Acohol)
• 836-43-1(p-Benzyloxybenzyl Alcohol)
• 1515-81-7(p-(Methoxymethyl)anisole)
• 3769-41-3(3-(Benzyloxy)phenol)
• 946-80-5(Benzyl phenyl ether)
• 176650-92-3(3,5-Bis(3,5-dimethoxybenzyloxy)benzyl Alcohol)
• 705-76-0(3,5-Dimethoxybenzyl alcohol)
• 103-16-2(Monobenzone)