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Catalog Number:
24623
CAS Number:
4488-22-6
1,1'-Binaphthyl-2,2'-diamine
Purity:
≥ 99% (HPLC)
Synonym(s):
2,2-Diamino-1,1'-binaphthalene
Documents
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Product Information

1,1'-Binaphthyl-2,2'-diamine is a versatile compound known for its unique chiral properties, making it an essential building block in asymmetric synthesis and catalysis. This compound, often utilized in the production of chiral ligands, plays a crucial role in various chemical reactions, including enantioselective transformations. Its ability to facilitate the formation of complex molecules with high specificity makes it invaluable in the pharmaceutical industry, particularly in the development of novel drugs and therapeutic agents. Researchers have also explored its applications in organic electronics and materials science, where its structural characteristics contribute to enhanced performance in devices such as organic light-emitting diodes (OLEDs).

The compound's stability and reactivity offer significant advantages over similar compounds, allowing for more efficient synthesis processes and improved yields. Its relevance extends to academic research, where it serves as a key reagent in studying reaction mechanisms and developing new synthetic methodologies. With its broad range of applications and benefits, 1,1'-Binaphthyl-2,2'-diamine is a vital resource for professionals seeking to innovate and advance their work in chemistry and related fields.

Synonyms
2,2-Diamino-1,1'-binaphthalene
CAS Number
4488-22-6
Purity
≥ 99% (HPLC)
Molecular Formula
C20H16N2
Molecular Weight
284.36
MDL Number
MFCD00145204
PubChem ID
20571
Melting Point
183-192 ?C
Appearance
White crystal
Conditions
Store at 0-8 °C
General Information
Synonyms
2,2-Diamino-1,1'-binaphthalene
CAS Number
4488-22-6
Purity
≥ 99% (HPLC)
Molecular Formula
C20H16N2
Molecular Weight
284.36
MDL Number
MFCD00145204
PubChem ID
20571
Melting Point
183-192 ?C
Appearance
White crystal
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,1'-Binaphthyl-2,2'-diamine is widely utilized in research focused on:

  • Chiral Catalysis: This compound serves as a chiral ligand in asymmetric synthesis, enhancing the selectivity and efficiency of reactions in the pharmaceutical industry.
  • Organic Electronics: It is used in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics, contributing to advancements in energy-efficient display technologies.
  • Drug Development: Researchers employ this chemical in the synthesis of various bioactive compounds, aiding in the discovery of new therapeutic agents.
  • Polymer Chemistry: It acts as a building block for creating novel polymers with unique properties, useful in materials science and engineering applications.
  • Analytical Chemistry: The compound is utilized in the development of sensitive detection methods for environmental monitoring and quality control in various industries.

Citations