52311-42-9

Basic information

• Product Name: 2-AMINO-4,4-BIPYRIDYL
• Synonyms: 2-AMINO-4,4-BIPYRIDYL;4-(pyridin-4-yl)pyridin-2-amine;2-Amino-4-(4-pyridyl)pyridine;[4,4'-Bipyridin]-2-amine
• CAS NO: 52311-42-9
• Molecular Formula: C₁₀H₉N₃
• Molecular Weight: 171.2
• EINECS: 604-604-1
• Mol File: 52311-42-9.mol

Chemical Properties

• Boiling Point: 356.4±32.0 °C(Predicted)
• Appearance: /
• Density: 1.193
• Storage Temp.: 2-8°C(protect from light)
• PKA: 4.84±0.11(Predicted)
• CAS DataBase Reference: 2-AMINO-4,4-BIPYRIDYL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-AMINO-4,4-BIPYRIDYL(52311-42-9)
• EPA Substance Registry System: 2-AMINO-4,4-BIPYRIDYL(52311-42-9)

Safety Data

• Hazardous Substances Data: 52311-42-9(Hazardous Substances Data)

Usage

Uses

Used in Coordination Chemistry:
2-AMINO-4,4-BIPYRIDYL is used as a ligand for forming stable complexes with transition metals. Its ability to coordinate with these metals is crucial for various applications in this field, including the development of catalysts and the study of metal complexes' properties.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2-AMINO-4,4-BIPYRIDYL plays a role in the formation of new organic compounds. Its unique structure and reactivity contribute to the synthesis of a variety of organic molecules, expanding the scope of chemical reactions and products.
Used in Catalyst Development:
2-AMINO-4,4-BIPYRIDYL has been studied for its potential use as a catalyst in chemical reactions. Its ability to form complexes with metals and influence reaction pathways makes it a promising candidate for enhancing the efficiency and selectivity of certain reactions.
Used in Material Science:
As a building block for the development of new materials, 2-AMINO-4,4-BIPYRIDYL contributes to the creation of innovative materials with unique properties. Its incorporation into materials can lead to advancements in areas such as electronics, pharmaceuticals, and other industries that benefit from novel materials with specific characteristics.

Upstream product

• 53344-73-3 4-(2-chloropyridin-4-yl)pyridine 
• 553-26-4 4,4'-bipyridine 

Downstream Products

• 622402-46-4 3-phenyl-7-pyridin-4-yl-imidazo[1,2-a]pyridine 
• 622402-48-6 4-(3-phenyl-imidazo[1,2-a]pyridin-7-yl)-1H-pyridin-2-one 

Relevant articles and documents

Design and synthesis of 3,7-diarylimidazopyridines as inhibitors of the VEGF-receptor KDR

3,7-Diarylsubstituted imidazopyridines were designed and developed as a new class of KDR kinase inhibitors. A variety of imidazopyridines were synthesized and potent inhibitors of KDR kinase activity were identified with good aqueous solubility.

Substituted pyridine and pyridazine compounds and methods of use

Selected novel substituted pyridine and pyridazine compounds are effective for prophylaxis and treatment of diseases, such as TNF-α, IL-1β, IL-6 and/or IL-8 mediated diseases, and other maladies, such as cancer, pain and diabetes. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving inflammation, cancer, pain, diabetes and the like. The subject invention also relates to processes for making such compounds as well as to intermediates useful in such processes.