S-1,2,3,4-Tetrahydro-1-naphthylamine CAS: 23357-52-0
Catalog Number | XD94230 |
Product Name | S-1,2,3,4-Tetrahydro-1-naphthylamine |
CAS | 23357-52-0 |
Molecular Formula | C10H13N |
Molecular Weight | 147.22 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
S-1,2,3,4-Tetrahydro-1-naphthylamine is a vital compound that finds usage in various industries due to its unique properties and versatile applications. It is an organic compound with a chiral center, meaning it exists in two mirror-image forms. The S-1,2,3,4-Tetrahydro-1-naphthylamine isomer specifically refers to the "S" or "sinister" form, which is the stereoisomer with the highest priority group on the left side of the chiral center.One significant application of S-1,2,3,4-Tetrahydro-1-naphthylamine is in the synthesis of pharmaceuticals. Chiral amines are crucial building blocks for many biologically active compounds and drugs. The presence of a chiral center in S-1,2,3,4-Tetrahydro-1-naphthylamine allows for the production of enantiomerically pure pharmaceuticals, which are compounds consisting of only one of the two mirror-image forms. This enantiopurity is important as it ensures maximum efficacy and reduces potential side effects in drugs. S-1,2,3,4-Tetrahydro-1-naphthylamine can serve as a versatile starting material to synthesize various chiral pharmaceutical intermediates, including antidepressants, antivirals, and antihistamines.Moreover, S-1,2,3,4-Tetrahydro-1-naphthylamine plays a significant role as a ligand in asymmetric catalysis. Chiral ligands are essential components in asymmetric synthesis, where chemists aim to selectively produce one enantiomer of a compound over its mirror image. Asymmetric catalysis is a key method to achieve this goal, and S-1,2,3,4-Tetrahydro-1-naphthylamine-based ligands have been utilized in various catalytic reactions, such as hydrogenations and cross-coupling reactions. The presence of a chiral ligand influences the stereochemistry of the reaction, enabling the production of complex molecules with high enantioselectivity.Additionally, S-1,2,3,4-Tetrahydro-1-naphthylamine finds application in the field of material science. Chiral molecules are crucial in the synthesis of materials with specific properties, such as chirality-dependent behavior and enantioselectivity. S-1,2,3,4-Tetrahydro-1-naphthylamine and its derivatives can be used as monomers to create chiral polymers, which have significance in various industries like electronics, optics, and catalysis. Chiral polymer materials find usage in the development of advanced technologies, such as optoelectronics and sensors.In summary, S-1,2,3,4-Tetrahydro-1-naphthylamine is a versatile compound with broad-ranging applications in pharmaceuticals, asymmetric catalysis, and material science. Its ability to exist as a chiral molecule allows for the production of enantiopure drugs with improved efficacy and reduced side effects. Additionally, S-1,2,3,4-Tetrahydro-1-naphthylamine's chiral nature enables the production of chiral polymers and the development of advanced materials. Overall, the unique properties of S-1,2,3,4-Tetrahydro-1-naphthylamine make it an essential component in various industries, driving advancements in healthcare, chemical synthesis, and materials engineering.