• 1. Excimer formation effects and trap-assisted charge recombination loss channels in organic solar cells of perylene diimide dimer acceptors?
  Min Kim,Jae-Joon Lee,Tengling Ye,Panagiotis E. Keivanidis,Kilwon Cho J. Mater. Chem. C, 2020,8, 1686-1696
• 2. Fe(ii)-Assisted one-pot synthesis of ultra-small core–shell Au–Pt nanoparticles as superior catalysts towards the HER and ORR?
  Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
• 3. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 4. Excited-state proton-coupled electron transfer within ion pairs?
  Gerald J. Meyer,Leif Hammarstr?m Chem. Sci., 2020,11, 3460-3473
• 5. Evidence of field induced slow magnetic relaxation in cis-[Co(hfac)2(H2O)2] exhibiting tri-axial anisotropy with a negative axial component?
  Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548

• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids and derivatives Benzoic acids

BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6): A Comprehensive Overview of Its Applications and Recent Research Findings

BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) is a specialized organic compound that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, characterized by its unique structural properties, exhibits a range of potential applications in various scientific domains. Understanding its chemical structure, synthesis methods, and emerging applications is crucial for researchers and professionals in the industry.

The molecular formula of BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) is C₉H₁₁NO₂, reflecting its composition of carbon, hydrogen, nitrogen, and oxygen atoms. The presence of both an amino group and a methyl group at specific positions on the benzene ring contributes to its distinct chemical behavior and reactivity. This structural configuration makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals.

In recent years, BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) has been studied for its potential role in drug discovery and development. Its ability to act as a precursor for more complex molecules has made it valuable in the synthesis of active pharmaceutical ingredients (APIs). Researchers have explored its utility in creating novel compounds with therapeutic properties, including those targeting neurological disorders and inflammatory conditions.

One of the most promising areas of research involving BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) is its application in designing bioactive molecules. Studies have demonstrated its role in the development of kinase inhibitors, which are crucial for treating cancers and other chronic diseases. The compound's ability to interact with specific biological targets makes it a valuable scaffold for medicinal chemists seeking to develop new drugs.

The synthesis of BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) involves multi-step organic reactions that require precise control over reaction conditions. Common synthetic routes include nucleophilic substitution reactions followed by functional group transformations. Advanced techniques such as catalytic hydrogenation and palladium-catalyzed cross-coupling reactions have been employed to improve yield and purity.

In addition to its pharmaceutical applications, BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) has shown potential in material science. Its structural properties make it suitable for use as a building block in the synthesis of polymers and specialty chemicals. Researchers are exploring its incorporation into materials that exhibit enhanced mechanical strength or unique electronic properties.

The environmental impact of BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) is another area of interest. While it is not classified as a hazardous substance, its persistence in certain environments raises concerns about potential ecological effects. Studies are ongoing to assess its degradation pathways and toxicity profiles, ensuring that its use remains safe and sustainable.

Economic considerations also play a significant role in the production and application of BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6). The cost-effectiveness of synthetic routes and the demand for derivatives influence industrial adoption. As research continues to uncover new uses for this compound, economic factors will likely drive further innovation in production methods.

The future prospects for BENZOIC ACID, 4-(AMINOMETHYL)-3-METHYL- (CAS No. 73831-12-6) are bright, with ongoing studies suggesting diverse applications across multiple industries. Its versatility as a chemical intermediate positions it as a key player in the development of next-generation pharmaceuticals and advanced materials. As researchers delve deeper into its potential, we can expect to see even more innovative uses emerge.

• 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)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 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)