25551-60-4

Basic information

• Product Name: N-(4-nitrophenyl)-4-pyridinamine
• Synonyms: N-(4-nitrophenyl)-4-pyridinamine
• CAS NO: 25551-60-4
• Molecular Weight: 215.211
• Mol File: 25551-60-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(4-nitrophenyl)-4-pyridinamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-nitrophenyl)-4-pyridinamine(25551-60-4)
• EPA Substance Registry System: N-(4-nitrophenyl)-4-pyridinamine(25551-60-4)

Safety Data

• Hazardous Substances Data: 25551-60-4(Hazardous Substances Data)

Upstream product

• 504-24-5 4-aminopyridine 
• 586-78-7 para-nitrophenyl bromide 
• 143-33-9 sodium cyanide 
• 22752-98-3 N-(4-pyridyl)pyridinium hydrochloride 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 60172-08-9 N₁-(4-pyridinyl)-1,4-benzenediamine 
• 1332220-29-7 4-tert-butyl-N-[[4-(4-pyridylamino)phenyl]-carbamothioyl]benzamide hydrochloride 
• 1020086-93-4 1-methyl-4-{4-[(4-nitroanilino)carbonyl]anilino}pyridinium tosylate 
• 1020086-91-2 C₁₉H₁₇N₄O₃⁽¹⁺⁾*Cl^(1-) 
• 23552-71-8 C₁₈H₁₄N₄O₃ 

Relevant articles and documents

AKT3 MODULATORS

Compounds of Formula Ia, lb, or Ic, Formula (Ia); Formula (Ib); or Formula (Ic), are described, where the various substituents are defined herein. The compounds can modulate a property or effect of Akt3 in vitro or in vivo, and can also be used, individually or in combination with other agents, in the prevention or treatment of a variety of conditions. Methods for synthesizing the compounds are described. Pharmaceutical compositions and methods of using these compounds or compositions, individually or in combination with other agents or compositions, in the prevention or treatment of a variety of conditions are also described.

SAR analysis of a series of acylthiourea derivatives possessing broad-spectrum antiviral activity

A series of acylthiourea derivatives were designed, synthesized, and evaluated for broad-spectrum antiviral activity with selected viruses from Poxviridae (vaccinia virus) and two different genera of the family Bunyaviridae (Rift Valley fever and La Cross

Synthetic Applications of N-N Linked Heterocycles. Part 15. A Facile Synthesis of 4-Pyridyl(aryl)amines via the Reaction between 4-Chloro-1-pyridiniopyridinium Salts and Aryl Amines

4-Chloro-1-pyridiniopyridinium salts (7) and (8) react with primary and secondary arylamines to give high yields of isolable 4-aryliminium salts (9) and (10).These are readily fragmented into 4-pyridyl(aryl)amines (11) and (12) in excellent yields on treatment with sodium cyanide or sodium salts of sulphonic acids.The method fails with the more basic aliphatic amines, since these apparently attack the 2-position of the chloropyridinium ring giving products resulting from ring-opening.Mechanisms of the reactions are discussed.