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551-09-7

N-(1-Naphthyl)ethylenediamine

Catalog#: AR00JOW5  |   CAS#: 551-09-7  |   MDL#: MFCD01631139  |   MF: C12H14N2  |   MW: 186.2530

Packsize Purity Price Availability Quantity
50mg 95% $79.00 Global Stock Buy Now Add To Cart
250mg 95% $178.00 Global Stock Buy Now Add To Cart
1g 95% $351.00 Global Stock Buy Now Add To Cart
5g 95% $1,159.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00JOW5
Chemical Name N-(1-Naphthyl)ethylenediamine
CAS Number 551-09-7
Molecular Formula C12H14N2
Molecular Weight 186.2530
MDL Number MFCD01631139
SMILES NCCNc1cccc2c1cccc2

N-(Naphthalen-1-yl)ethane-1,2-diamine, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and diverse applications. This compound acts as a vital building block in the creation of various organic molecules, owing to its ability to serve as a key intermediate in multiple synthetic pathways.One of the primary applications of N-(Naphthalen-1-yl)ethane-1,2-diamine in chemical synthesis is its role as a key reagent in the preparation of complex heterocyclic compounds. By reacting with suitable substrates under specific conditions, this compound facilitates the formation of diverse nitrogen-containing ring structures, which are crucial components in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, N-(Naphthalen-1-yl)ethane-1,2-diamine is known for its utility in the production of chiral ligands for asymmetric catalysis. Through selective functionalization of its amino groups or naphthalene moiety, this compound can be modified to generate ligands that enable the enantioselective synthesis of a wide range of organic compounds with high stereocontrol.Moreover, the versatility of N-(Naphthalen-1-yl)ethane-1,2-diamine extends to its use in coordinating metal ions in organometallic chemistry. By forming stable complexes with transition metals, this compound serves as a valuable ligand for catalytic reactions, such as cross-coupling reactions and metal-catalyzed transformations, enhancing the efficiency and selectivity of various synthetic processes.Overall, N-(Naphthalen-1-yl)ethane-1,2-diamine stands out as a crucial reagent in the realm of chemical synthesis, offering a wide range of applications from heterocyclic synthesis to asymmetric catalysis and organometallic chemistry. Its diverse functionalities and reactivity make it an indispensable tool for the creation of complex organic molecules with tailored properties and functionalities.
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