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Home  > 1,5-Diaminonaphthalene

AB57583

2243-62-1 | 1,5-Diaminonaphthalene

Packsize Purity Availability Price Discounted Price    Quantity
25g 98% in stock $8.00 $5.00 -   +
50g 98% in stock $12.00 $8.00 -   +
100g 98% in stock $19.00 $13.00 -   +
500g 98% in stock $70.00 $49.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB57583
Chemical Name: 1,5-Diaminonaphthalene
CAS Number: 2243-62-1
Molecular Formula: C10H10N2
Molecular Weight: 158.1998
MDL Number: MFCD00004029
SMILES: Nc1cccc2c1cccc2N
NSC Number: 401110

 

Computed Properties
Complexity: 140  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • Naphthalene-1,5-diamine, also known as 1,5-diaminonaphthalene, finds significant application in chemical synthesis as a versatile building block for the preparation of various organic compounds. This compound serves as a key intermediate in the synthesis of dyes, pigments, pharmaceuticals, and polymers. Its unique molecular structure allows for diverse functionalization reactions, enabling the creation of more complex molecules with tailored properties.In organic synthesis, Naphthalene-1,5-diamine is utilized in the production of azo dyes, which are widely used in textiles, plastics, and other industries for their vibrant and long-lasting coloration. By reacting with diazonium salts of aromatic amines, this compound participates in diazo coupling reactions to form azo compounds with azo linkage (-N=N-), a vital feature for color development.Moreover, Naphthalene-1,5-diamine serves as a key precursor in the synthesis of various pharmaceutical agents and agrochemicals. Through selective functionalization of its amino groups, researchers can introduce specific structural motifs that enhance the biological activity or target specificity of the resulting molecules. This compound also plays a crucial role in the production of polymeric materials, where it serves as a monomer for the synthesis of polyamides, polyimides, and other high-performance polymers.In summary, Naphthalene-1,5-diamine's significance in chemical synthesis lies in its ability to participate in a wide range of reactions, offering a valuable platform for the construction of diverse organic compounds with applications spanning from colorants to advanced materials.
Literature
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