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56138-96-6

2,6-Dibenzhydryl-4-methylaniline

Catalog#: AR01EG5U  |   CAS#: 56138-96-6  |   MDL#: MFCD23704470  |   MF: C33H29N  |   MW: 439.5901

Packsize Purity Price Availability Quantity
100mg 90% $12.00 Global Stock Buy Now Add To Cart
250mg 90% $18.00 Global Stock Buy Now Add To Cart
1g 90% $51.00 Global Stock Buy Now Add To Cart
5g 90% $182.00 Global Stock Buy Now Add To Cart
25g 90% $687.00 Global Stock Buy Now Add To Cart
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Catalog Number AR01EG5U
Chemical Name 2,6-Dibenzhydryl-4-methylaniline
CAS Number 56138-96-6
Molecular Formula C33H29N
Molecular Weight 439.5901
MDL Number MFCD23704470
SMILES Cc1cc(C(c2ccccc2)c2ccccc2)c(c(c1)C(c1ccccc1)c1ccccc1)N

2,6-Dibenzhydryl-4-methylaniline, also known as $name$, is a versatile compound widely utilized in chemical synthesis as a key building block in organic reactions. This aromatic amine compound is valued for its unique structural properties and reactivity, making it an essential component in the preparation of various specialty chemicals and pharmaceutical intermediates.In chemical synthesis, $name$ serves as a valuable starting material for the synthesis of diverse organic compounds due to its high degree of functionalization and compatibility with various reaction conditions. It can undergo a range of transformations such as electrophilic and nucleophilic substitutions, aromatic coupling reactions, and metal-catalyzed transformations, allowing for the efficient construction of complex molecular structures.One of the prominent applications of 2,6-Dibenzhydryl-4-methylaniline in chemical synthesis is as a building block for the preparation of novel pharmaceutical agents, agrochemicals, and advanced materials. Its versatile nature and ability to participate in selective functional group manipulations make it a valuable tool for organic chemists seeking to design and synthesize new molecules with tailored properties and functionalities.Additionally, $name$ can also be employed in the development of molecular probes, catalysts, and specialty polymers, showcasing its broad utility in diverse fields of organic chemistry. Its structural features, including the presence of aryl groups and aniline moiety, enable it to participate in key bond-forming reactions essential for the creation of structurally complex and biologically active compounds.Furthermore, the robust and tunable reactivity of 2,6-Dibenzhydryl-4-methylaniline makes it a valuable reagent for the construction of intricate molecular architectures with precise stereochemical control, facilitating the synthesis of chiral compounds and pharmaceutical substances with high optical purity.Overall, the versatile and synthetically useful properties of 2,6-Dibenzhydryl-4-methylaniline make it a valuable asset in the toolkit of synthetic chemists for the efficient and strategic construction of intricate organic molecules with diverse applications in pharmaceuticals, materials science, and chemical research.
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