• 1. An Assessment of the Laminar Hypersonic Double-Cone Experiments in the LENS-XX Tunnel
  JaideepRay,PatrickBlonigan,EricT.Phipps,KathrynMaupin
• 2. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
  Quan Xiang,Yiqin Chen,Zhiqin Li,Kaixi Bi,Guanhua Zhang,Huigao Duan Nanoscale, 2016,8, 19541-19550
• 3. An approach to asymmetric synthesis of β-aryl alanines by Pd(0)-catalyzed cross-coupling and cyanate-to-isocyanate rearrangement?
  Piotr Szcze?niak,Sebastian Stecko RSC Adv., 2015,5, 30882-30888
• 4. An astrophysically-relevant mechanism for amino acid enantiomer enrichment
  Stephen P. Fletcher,Richard B. C. Jagt,Ben L. Feringa Chem. Commun., 2007, 2578-2580
• 5. An integrated system for field analysis of Cd(ii) and Pb(ii) via preconcentration using nano-TiO2/cellulose paper composite and subsequent detection with a portable X-ray fluorescence spectrometer?
  Xiaofeng Lin RSC Adv., 2016,6, 9002-9006

2-Amino-4,5-Dimethylbenzaldehyde: A Comprehensive Overview

2-Amino-4,5-Dimethylbenzaldehyde, also known by its CAS registry number CAS No. 65176-91-2, is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound is characterized by its unique structure, which includes an amino group (-NH?) attached to the second carbon of a benzene ring and two methyl groups (-CH?) on the fourth and fifth carbons. The presence of these substituents imparts distinctive chemical and physical properties to the molecule, making it a valuable compound in both academic research and industrial applications.

The synthesis of 2-Amino-4,5-Dimethylbenzaldehyde has been extensively studied, with researchers exploring various methods to optimize its production. Recent advancements in catalytic chemistry have enabled the development of more efficient synthesis pathways, reducing the environmental footprint and cost associated with its manufacturing. For instance, the use of transition metal catalysts has been reported to significantly enhance the yield of this compound during the coupling reactions.

In terms of chemical properties, 2-Amino-4,5-Dimethylbenzaldehyde exhibits a high degree of stability under normal conditions, though it is prone to oxidation when exposed to strong oxidizing agents or under specific reaction conditions. Its solubility in common solvents such as water and ethanol has been well-documented, making it suitable for use in various solution-based reactions. Recent studies have also highlighted its potential as a precursor for synthesizing advanced materials, including metal-organic frameworks (MOFs) and coordination polymers.

The application of 2-Amino-4,5-Dimethylbenzaldehyde extends across multiple disciplines. In pharmaceutical research, it has been utilized as an intermediate in the synthesis of bioactive compounds with potential therapeutic applications. For example, researchers have explored its role in developing anti-inflammatory and anticancer agents by leveraging its ability to form stable complexes with metal ions. Additionally, in the field of materials science, this compound has been employed as a building block for constructing porous materials with high surface area and catalytic activity.

The environmental impact of 2-Amino-4,5-Dimethylbenzaldehyde has also garnered attention in recent years. Studies have investigated its biodegradability and toxicity profiles under various environmental conditions. Findings suggest that while it is not inherently hazardous under normal usage conditions, proper handling and disposal protocols should be followed to minimize any potential ecological risks.

In conclusion, 2-Amino-4,5-Dimethylbenzaldehyde, CAS No. 65176-91-2, stands as a testament to the ingenuity of modern chemical synthesis and its wide-ranging applications. With ongoing research into its properties and potential uses, this compound continues to play a pivotal role in advancing both fundamental and applied sciences.

• 109467-00-7(2-Amino-5-methylbenzaldehyde)
• 70128-12-0(2-amino-3,5-dimethylbenzaldehyde)
• 529-23-7(2-Aminobenzaldehyde)
• 59236-38-3(2-amino-4-methyl-benzaldehyde)
• 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)