1932-35-0

Basic information

• Product Name: Urea,N-phenyl-N'-4-pyridinyl-
• CAS NO: 1932-35-0
• Molecular Weight: 213.239
• Mol File: 1932-35-0.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: Urea,N-phenyl-N'-4-pyridinyl- (CAS DataBase Reference)
• NIST Chemistry Reference: Urea,N-phenyl-N'-4-pyridinyl- (1932-35-0)
• EPA Substance Registry System: Urea,N-phenyl-N'-4-pyridinyl- (1932-35-0)

Safety Data

• Hazardous Substances Data: 1932-35-0(Hazardous Substances Data)

Usage

General Description

Urea, N-phenyl-N'-4-pyridinyl- is a chemical compound with the molecular formula C11H11N3O. It is a derivative of urea and contains a phenyl and pyridinyl group. Urea,N-phenyl-N'-4-pyridinyl- is used in the production of pharmaceuticals and agrochemicals, as well as in organic synthesis and research. It has potential applications in the field of medicinal chemistry and has been studied for its biological activities. Urea, N-phenyl-N'-4-pyridinyl- may also have other industrial uses, such as in the development of new materials or as a reagent in chemical reactions. Overall, this compound has diverse potential applications and is of interest to researchers and industry professionals.

Upstream product

• 504-24-5 4-aminopyridine 
• 103-71-9 phenyl isocyanate 
• 4013-73-4 isonicotinoyl azide 
• 62-53-3 aniline 
• 626-61-9 4-Chloropyridine 
• 64-10-8 phenyl carbamate 
• 55-22-1 pyridine-4-carboxylic acid 
• 1120-87-2 4-bromopyridin 
• 1692-15-5 4-pyridylboronic acid 
• 201230-82-2 carbon monoxide 

Downstream Products

• 862886-16-6 [(1-phenyl-3-pyridine-4-yl-urea)2Ag]PF₆ 
• 140367-31-3 5-tert-Butyl-1-phenyl-3-pyridin-4-yl-[1,3,5]triazinan-2-one 

Relevant articles and documents

New broad-spectrum parenteral cephalosporins exhibiting potent activity against both methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa. Part 3: 7β-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2- ethoxyiminoacetamido] cephalosporins beari

Among the prepared C-3′ substituted-pyridinium cephalosporins, a series of 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-ethoxyiminoacetamido] cephalosporins bearing 4-[3-(aminoalkyl)-ureido]-1-pyridinium at C-3′ showed highly potent antibacterial activity agai

Substituent effect of N-aryl-N′-pyridyl ureas as thermal latent initiators on ring-opening polymerization of epoxide

A series of N-aryl-N′-pyridyl ureas were synthesized by the reactions of 4-aminopyridine (4AP) with the corresponding isocyanates such as phenyl isocyanate, 4-methylphenyl isocyanate, 4-methoxyphenyl isocyanate, 4-chlorophenyl isocyanate, 4-(trifluorometh

Cu(acac)2-catalyzed N-arylations of phenylurea with aryl boronic acid

Cu(acac)2 activates aryl boronic acids for the reaction with NH2-phenylurea without additional ligand and heating. The procedure is simple, general, ligand-free, milder than the palladium-catalyzed arylation, and avoids the use of toxic phosphine ligands. Copyright Taylor & Francis Group, LLC.