Product Description
We are a supplier of (1S,2S)-1,2-Diamino-1,2-diphenylethane. These are formulated by using high quality ingredients that is obtained from reliable and trusted market vender. Available with us at very competitive price.
CAS No.: 29841-69-8
Molecular Formula: C14H16N2
Molecular Weight: 212.29
AI Product Description
*The following content is generated by AI and is for reference only.
(1S,2S)-1,2-Diamino-1,2-diphenylethane is a chiral organic compound belonging to the class of vicinal diamines. Its molecular formula is C14H16N2, and it is widely recognized by the CAS number 38905-37-0. This molecule features two phenyl groups attached to adjacent carbon atoms, each bearing an amino group, with a specific stereochemical configuration defined as (1S,2S). The enantiomeric purity of this compound makes it a valuable reagent in asymmetric synthesis and chiral resolution processes.
The primary application of (1S,2S)-1,2-diamino-1,2-diphenylethane lies in its role as a chiral ligand or auxiliary in organometallic chemistry. It is frequently employed to coordinate with transition metals, forming stable complexes that catalyze enantioselective reactions. These catalytic systems are crucial for synthesizing optically active pharmaceutical intermediates, agrochemicals, and fine chemicals where stereochemistry dictates biological activity. By utilizing this specific enantiomer, chemists can achieve high levels of stereoselectivity, minimizing the formation of unwanted isomers and reducing purification costs.
Beyond catalysis, this diamine serves as a key building block for constructing complex heterocyclic structures, including bis-oxazolines and other nitrogen-containing macrocycles. Its rigid backbone and well-defined chirality allow for predictable coordination geometries, facilitating the design of novel catalysts for hydrogenation, epoxidation, and aldol-type reactions. Furthermore, it acts as a standard reference material in analytical chemistry for validating chiral separation techniques such as HPLC and capillary electrophoresis. Due to its sensitivity to oxidation and moisture, handling requires inert atmospheres and proper storage conditions to maintain stability. Overall, (1S,2S)-1,2-diamino-1,2-diphenylethane represents a fundamental tool in modern synthetic methodology, enabling the efficient production of high-value chiral compounds essential for advanced materials and medicinal research. Its versatility continues to drive innovation in the development of sustainable and precise chemical manufacturing processes across various industrial sectors.
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