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• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Aralkylamines
• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Aralkylamines

Comprehensive Overview of (5-Methylthien-2-yl)methylamine Hydrochloride (CAS No. 171661-55-5)

(5-Methylthien-2-yl)methylamine Hydrochloride is a specialized organic compound with significant applications in pharmaceutical research and chemical synthesis. Its CAS number, 171661-55-5, serves as a unique identifier in global chemical databases, ensuring precise tracking and regulatory compliance. This compound, often abbreviated as 5-MTMA HCl, is widely recognized for its role as a versatile intermediate in the development of bioactive molecules, particularly in the fields of neurology and metabolic studies.

The molecular structure of (5-Methylthien-2-yl)methylamine Hydrochloride features a thiophene ring substituted with a methyl group at the 5-position, coupled with an amine functional group. This configuration enhances its reactivity, making it valuable for cross-coupling reactions and N-functionalization processes. Researchers frequently explore its potential in designing small-molecule inhibitors and ligands for receptor targeting, aligning with current trends in precision medicine and drug discovery.

In recent years, the demand for high-purity intermediates like 171661-55-5 has surged due to advancements in high-throughput screening (HTS) and combinatorial chemistry. Laboratories prioritize compounds with well-documented synthetic pathways and scalability, both of which are associated with this product. Its hydrochloride salt form improves stability and solubility, addressing common challenges in formulation development.

From an industrial perspective, (5-Methylthien-2-yl)methylamine Hydrochloride is synthesized under controlled conditions to meet Good Manufacturing Practice (GMP) standards. Analytical techniques such as HPLC, NMR, and mass spectrometry are employed to verify its purity, often exceeding 98%. These quality assurances cater to the stringent requirements of contract research organizations (CROs) and academic institutions.

Environmental and safety considerations are integral to its handling. While not classified as hazardous under major regulatory frameworks, proper laboratory safety protocols—including ventilation and personal protective equipment (PPE)—are recommended. This aligns with the growing emphasis on green chemistry and sustainable practices in chemical production.

Emerging applications of CAS 171661-55-5 include its exploration in neurotransmitter modulation studies, particularly concerning serotonin and dopamine pathways. Such investigations resonate with public interest in mental health therapeutics and cognitive enhancement, topics frequently searched in scientific and medical forums.

In summary, (5-Methylthien-2-yl)methylamine Hydrochloride exemplifies the intersection of structural versatility and functional utility in modern chemistry. Its relevance to cutting-edge research and adherence to quality benchmarks position it as a critical asset for scientists navigating the complexities of molecular design and therapeutic innovation.

• 27757-85-3(thiophen-2-ylmethanamine)
• 58255-18-8(methyl(thiophen-2-ylmethyl)amine)
• 58703-21-2(bis(thiophen-2-ylmethyl)amine)
• 7404-67-3(2-Methylaminomethylthiophene Hydrochloride)
• 912569-78-9(2-Methyl-5-(methylamino)methylthiophene Hydrochloride)
• 58255-25-7(N-Ethyl-(2-thienylmethyl)amine)
• 26019-17-0(N,N-Dimethyl-1-(thiophen-2-yl)methanamine)
• 887592-30-5((5-methylthiophen-2-yl)methylhydrazine)
• 336624-10-3(Bis(2-thiophenemethyl)amine hydrochloride)
• 104163-34-0((5-Methylthiophen-2-yl)methanamine)