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Catalog Number:
47519
CAS Number:
771-97-1
2,3-Diaminonaphthalene
Purity:
≥ 98% (GC)
Synonym(s):
2,3-Naphthalenediamine
Documents
$64.80 /100MG
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Product Information

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.

Synonyms
2,3-Naphthalenediamine
CAS Number
771-97-1
Purity
≥ 98% (GC)
Molecular Formula
C10H10N2
Molecular Weight
158.2
MDL Number
MFCD00004116
PubChem ID
69872
Melting Point
198 °C
Density
1.096
Appearance
White to yellow to orange powder
Conditions
Store at 2 - 8 °C, under inert gas
General Information
Synonyms
2,3-Naphthalenediamine
CAS Number
771-97-1
Purity
≥ 98% (GC)
Molecular Formula
C10H10N2
Molecular Weight
158.2
MDL Number
MFCD00004116
PubChem ID
69872
Melting Point
198 °C
Density
1.096
Appearance
White to yellow to orange powder
Conditions
Store at 2 - 8 °C, under inert gas
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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