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Catalog Number:
47519
CAS Number:
771-97-1
2,3-Diaminonaphtalène
Purity:
≥ 98% (CG)
Synonym(s):
2,3-Naphtalènediamine
Documents
$64.80 /100 mg
Taille
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Informations sur le produit

2,3-Diaminonaphthalene is a versatile organic compound known for its significant role in various industrial and research applications. This compound, with its unique structure, serves as a crucial intermediate in the synthesis of dyes, pigments, and pharmaceuticals. Its ability to undergo various chemical reactions makes it an essential building block in the production of complex organic molecules. Researchers often utilize 2,3-Diaminonaphthalene in the development of advanced materials, including conductive polymers and organic semiconductors, due to its excellent electronic properties.

In addition to its applications in the dye and pigment industry, 2,3-Diaminonaphthalene is also employed in the synthesis of heterocyclic compounds, which are vital in medicinal chemistry. Its reactivity and functional groups allow for the modification of existing compounds, leading to the discovery of new therapeutic agents. The compound's stability and ease of handling further enhance its appeal for laboratory use, making it a preferred choice for professionals seeking reliable and effective chemical solutions.

Numéro CAS 
771-97-1
Formule moléculaire
C10H10N2
Poids moléculaire 
158.2
Point de fusion 
198 °C
Informations générales
Numéro CAS 
771-97-1
Formule moléculaire
C10H10N2
Poids moléculaire 
158.2
Point de fusion 
198 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

2,3-Diaminonaphthalene is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, including dyes and pharmaceuticals, enhancing the efficiency of chemical reactions.
  • Fluorescent Dyes: It is used in the production of fluorescent dyes, which are essential in biological imaging and diagnostics, allowing researchers to visualize cellular processes with high precision.
  • Polymer Chemistry: The compound is incorporated into polymer formulations to improve thermal stability and mechanical properties, making it valuable in the manufacturing of high-performance materials.
  • Analytical Chemistry: It acts as a reagent in analytical methods, such as spectrophotometry, for detecting and quantifying various analytes, providing reliable results in quality control processes.
  • Biological Research: 2,3-Diaminonaphthalene is studied for its potential applications in cancer research, as it may influence cellular pathways, offering insights into therapeutic strategies.

Citations