107676-55-1

Basic information

• Product Name: 3-(4-fluorophenyl)-1-(4-methoxyphenyl)urea
• Synonyms: 3-(4-fluorophenyl)-1-(4-methoxyphenyl)urea
• CAS NO: 107676-55-1
• Molecular Weight: 260.268
• Mol File: 107676-55-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-(4-fluorophenyl)-1-(4-methoxyphenyl)urea(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-fluorophenyl)-1-(4-methoxyphenyl)urea(107676-55-1)
• EPA Substance Registry System: 3-(4-fluorophenyl)-1-(4-methoxyphenyl)urea(107676-55-1)

Safety Data

• Hazardous Substances Data: 107676-55-1(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 1195-45-5 para-fluorophenyl isocyanate 
• 371-40-4 4-fluoroaniline 
• 201230-82-2 carbon monoxide 
• 3296-02-4 p-azidofluorobenzene 
• 696-62-8 para-iodoanisole 
• 659-30-3 1-(4-fluorophenyl)urea 
• 352-34-1 4-fluoro-1-iodobenzene 
• 1566-42-3 p-anisidine urea 

Downstream Products

• 107676-72-2 3-(4-fluorophenyl)-1-(4-methoxyphenyl)-3-nitrosourea 
• 107676-71-1 C₁₄H₁₂FN₃O₃ 

Relevant articles and documents

Pd/C Catalyzed Carbonylation of Azides in the Presence of Amines

A facile and efficient Pd/C-catalyzed carbonylation of both aliphatic and aromatic azides in the presence of amines is reported. Serving as the widely existed fragments in an array of biological pharmaceuticals, functionalized unsymmetrical ureas were str

Microwave assisted, ligand free, copper catalyzed reaction of aryl halides with phenyl urea

The ligand free coupling reaction of phenyl urea with different functionalized aryl halides in the presence of air stable Cu2O and t-BuOK as a base gives symmetrical and unsymmetrical diarylureas in relatively high yields. This method is milder than the palladium catalyzed arylation and avoids the use of toxic phosphine ligand.

Substituent effects on nitrosation of 1,3-diarylureas with nitrosyl chloride, dinitrogen trioxide, and dinitrogen tetroxide

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