• 1. Evolution of hierarchical porous structures in supramolecular guest–host hydrogels?
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  Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544

• 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

Comprehensive Overview of 5-Aminomethyl-2-methyl-benzoic acid (CAS No. 733690-37-4): Properties, Applications, and Industry Insights

5-Aminomethyl-2-methyl-benzoic acid (CAS No. 733690-37-4) is a specialized organic compound gaining attention in pharmaceutical and chemical research due to its unique structural features. This benzoic acid derivative is characterized by an aminomethyl group at the 5-position and a methyl group at the 2-position, making it a versatile intermediate for synthesizing more complex molecules. Researchers and manufacturers frequently search for "5-Aminomethyl-2-methyl-benzoic acid synthesis" or "CAS 733690-37-4 suppliers," reflecting its growing demand in fine chemical production.

The compound’s molecular formula, C₉H₁₁NO₂, and molecular weight of 165.19 g/mol position it as a critical building block in medicinal chemistry. Recent studies highlight its potential in designing small-molecule inhibitors and peptide mimetics, aligning with the trending focus on targeted drug discovery. Searches like "5-Aminomethyl-2-methyl-benzoic acid applications in drug development" underscore its relevance in addressing diseases such as metabolic disorders and inflammation.

From a physicochemical perspective, 5-Aminomethyl-2-methyl-benzoic acid typically appears as a white to off-white crystalline powder with moderate solubility in polar solvents like water and ethanol. Its stability under ambient conditions makes it suitable for industrial-scale handling, though proper storage away from moisture is recommended. Queries such as "CAS 733690-37-4 solubility and stability" are common among formulation scientists optimizing delivery systems.

In the context of green chemistry, this compound’s efficient synthetic routes—often involving catalytic hydrogenation or reductive amination—are frequently discussed. Environmental concerns have spurred interest in "sustainable production of 5-Aminomethyl-2-methyl-benzoic acid," with researchers exploring biocatalysts and solvent-free methods to reduce waste. Such innovations align with global regulatory trends emphasizing cleaner manufacturing processes.

Beyond pharmaceuticals, 5-Aminomethyl-2-methyl-benzoic acid finds niche applications in agrochemicals and material science. Its aromatic core and functional groups enable modifications for crop protection agents or polymer additives. Industry professionals often investigate "CAS 733690-37-4 cross-coupling reactions" to exploit its reactivity in creating advanced materials.

Analytical techniques like HPLC, NMR, and mass spectrometry are essential for quality control of this compound. Rigorous purity standards (>98%) are demanded in high-value applications, driving searches for "5-Aminomethyl-2-methyl-benzoic acid analytical methods." Vendors emphasizing batch-to-batch consistency gain traction in competitive markets.

As the life sciences sector grows, the demand for custom synthesis and contract manufacturing of intermediates like 5-Aminomethyl-2-methyl-benzoic acid is projected to rise. Strategic partnerships between academic institutions and chemical enterprises are accelerating its adoption in next-generation therapeutics, ensuring this compound remains a focal point in R&D investment.

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• 2393-20-6(3-(Aminomethyl)benzoic acid)
• 106677-32-1(Benzoic acid, 2-(aminomethyl)-5-methyl-, nickel(2+) salt (2:1))
• 7499-18-5( )
• 10017-39-7(2-(AMINOMETHYL)BENZOIC ACID HYDROCHLORIDE)
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• 25672-97-3(2-(Aminomethyl)benzoic acid)
• 105995-43-5(3,5-Bis(aminomethyl)benzoic acid)