• 1. Evolution of dealloying induced strain in nanoporous gold crystals?
  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 2. Estimates of hydride ion stability in condensed systems: energy of formation and solvation in aqueous and polar-organic solvents
  Craig A. Kelly,David R. Rosseinsky Phys. Chem. Chem. Phys., 2001,3, 2086-2090
• 3. Exceptionally high temperature spin crossover in amide-functionalised 2,6-bis(pyrazol-1-yl)pyridine iron(ii) complex revealed by variable temperature Raman spectroscopy and single crystal X-ray diffraction?
  Max Attwood,Hiroki Akutsu,Lee Martin,Toby J. Blundell,Pierre Le Maguere,Scott S. Turner Dalton Trans., 2021,50, 11843-11851
• 4. Establishing the accuracy of position-specific carbon isotope analysis of propane by GC-pyrolysis-GC-IRMS
  ChangjieLiu,PengLiu,XiaofengWang,XiaoqiangLi,JuskeHorita
• 5. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245

Comprehensive Guide to BENZENEMETHANAMINE, 2,4-DIBROMO- (CAS No. 64382-94-1): Properties, Applications, and Market Insights

BENZENEMETHANAMINE, 2,4-DIBROMO- (CAS No. 64382-94-1) is a brominated aromatic amine with significant relevance in organic synthesis and specialty chemical applications. This compound, also known as 2,4-Dibromobenzylamine, features a benzene ring substituted with two bromine atoms at the 2 and 4 positions and an aminomethyl group. Its unique structure makes it a valuable intermediate in pharmaceuticals, agrochemicals, and material science.

The molecular formula of BENZENEMETHANAMINE, 2,4-DIBROMO- is C₇H₇Br₂N, with a molecular weight of 264.95 g/mol. Its physical properties include a white to light yellow crystalline powder appearance, moderate solubility in organic solvents like ethanol and dichloromethane, and limited solubility in water. The presence of bromine atoms enhances its reactivity, particularly in electrophilic aromatic substitution and nucleophilic reactions.

One of the primary applications of BENZENEMETHANAMINE, 2,4-DIBROMO- is as a building block in pharmaceutical synthesis. Researchers utilize it to develop active pharmaceutical ingredients (APIs) for treating various conditions. For instance, it serves as a precursor in the synthesis of brominated analogs of biologically active molecules, which are increasingly explored in drug discovery due to their enhanced metabolic stability and binding affinity.

In the agrochemical industry, 2,4-Dibromobenzylamine is employed to formulate herbicides and fungicides. Its brominated structure contributes to the efficacy of these compounds by improving their interaction with target enzymes or receptors in pests and pathogens. Recent trends in sustainable agriculture have spurred interest in developing eco-friendly brominated compounds, positioning BENZENEMETHANAMINE, 2,4-DIBROMO- as a key intermediate.

Material science is another domain where BENZENEMETHANAMINE, 2,4-DIBROMO- finds utility. It is used in the synthesis of advanced polymers and flame retardants. The bromine atoms impart flame-retardant properties, making it valuable for producing materials with enhanced safety profiles, such as those used in electronics and construction. With the growing demand for flame-retardant materials in electric vehicles (EVs) and renewable energy systems, the relevance of this compound is expected to rise.

The market dynamics for BENZENEMETHANAMINE, 2,4-DIBROMO- reflect increasing demand from Asia-Pacific regions, particularly China and India, where pharmaceutical and agrochemical industries are expanding rapidly. Global suppliers are focusing on optimizing production processes to meet regulatory standards and ensure consistent quality. Environmental regulations, such as REACH and TSCA, govern its manufacturing and handling, emphasizing the need for sustainable practices.

Researchers and industry professionals frequently search for information on synthesis methods of 2,4-Dibromobenzylamine, safety data sheets (SDS), and suppliers of CAS 64382-94-1. Recent studies highlight innovative catalytic approaches to synthesize this compound with higher yields and lower environmental impact. Additionally, advancements in green chemistry have led to the development of solvent-free or water-based reaction conditions, aligning with global sustainability goals.

For laboratories and industrial users, proper storage and handling of BENZENEMETHANAMINE, 2,4-DIBROMO- are critical. It should be stored in a cool, dry place away from oxidizing agents and strong acids. Personal protective equipment (PPE), including gloves and goggles, is recommended during handling to ensure safety. Regulatory compliance and adherence to good laboratory practices (GLP) are essential to mitigate risks.

In summary, BENZENEMETHANAMINE, 2,4-DIBROMO- (CAS No. 64382-94-1) is a versatile compound with broad applications in pharmaceuticals, agrochemicals, and material science. Its unique chemical properties and growing market demand underscore its importance in modern chemistry. As research continues to explore new applications and sustainable synthesis methods, this compound is poised to play a pivotal role in addressing contemporary challenges in science and industry.

• 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)