57709-64-5

Basic information

• Product Name: N-(2-AMINOPHENYL)-N''-PHENYLUREA
• Synonyms: N-(2-AMINOPHENYL)-N''-PHENYLUREA
• CAS NO: 57709-64-5
• Molecular Formula: C₁₃H₁₃N₃O
• Molecular Weight: 227.26
• Mol File: 57709-64-5.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(2-AMINOPHENYL)-N''-PHENYLUREA(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-AMINOPHENYL)-N''-PHENYLUREA(57709-64-5)
• EPA Substance Registry System: N-(2-AMINOPHENYL)-N''-PHENYLUREA(57709-64-5)

Safety Data

• Hazardous Substances Data: 57709-64-5(Hazardous Substances Data)

Upstream product

• 103-71-9 phenyl isocyanate 
• 95-54-5 1,2-diamino-benzene 
• 71-43-2 benzene 

Downstream Products

• 615-16-7 1,3-dihydro-2H-benzimidazol-2-one 
• 62-53-3 aniline 
• 95-54-5 1,2-diamino-benzene 
• 1050211-40-9 1-(2-(phenylureido)phenyl)-3-ferrocenylurea 
• 1050211-31-8 1-(2-(ferrocenecarboxamido)phenyl)-3-phenylurea 
• 1401033-05-3 N¹-[N-(4-nitrophenyl)thiocarbamoyl]-N²-[N-phenylcarbamoyl]-1,2-diaminobenzene 
• 1401033-04-2 N¹-[N-(4-chlorophenyl)thiocarbamoyl]-N²-[N-phenylcarbamoyl]-1,2-diaminobenzene 
• 1345145-29-0 C₄₃H₃₈N₆O₄S₂ 
• 86298-24-0 N-phenyl-1H-benzo[d][1,2,3]triazole-1-carboxamide 
• 215917-77-4 N-[2-(3-phenylureido)phenyl]benzene-sulfonamide 
• 2589-21-1 1,1'-dibutyl-3-phenylurea 
• 130632-42-7 C₃₇H₆₄N₆OP₂ 
• 101-42-8 fenuron 
• 1014-72-8 1-phenyl-3,3-diethylurea 

Relevant articles and documents

Broad Scope and High-Yield Access to Unsymmetrical Acyclic [11C]Ureas for Biomedical Imaging from [11C]Carbonyl Difluoride

Effective methods are needed for labelling acyclic ureas with carbon-11 (t1/2=20.4 min) as potential radiotracers for biomedical imaging with positron emission tomography (PET). Herein, we describe the rapid and high-yield syntheses of unsymmet

RECORDING MATERIAL PRODUCED USING NON-PHENOL COMPOUND

An object of the present invention is to provide a recording material or a recording sheet using, as a color-developing agent, a non-phenol compound that is a safe compound in no danger of corresponding to an endocrine disruptor and is good in color devel

Desymmetrisation of aromatic diamines and synthesis of non-symmetrical thiourea derivatives by click-mechanochemistry

ortho- and para-Phenylenediamines were desymmetrised and quantitatively transformed into mono- and bis-(thio)ureas or mixed thiourea-ureas through a one-pot mechanochemical click reaction sequence; mechanochemical desymmetrisation proceeds quantitatively