859807-24-2

Basic information

• Product Name: (4-nitro-phenyl)-carbamic acid trichloromethyl ester
• Synonyms: (4-nitro-phenyl)-carbamic acid trichloromethyl ester
• CAS NO: 859807-24-2
• Molecular Weight: 299.498
• Mol File: 859807-24-2.mol

Chemical Properties

• CAS DataBase Reference: (4-nitro-phenyl)-carbamic acid trichloromethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (4-nitro-phenyl)-carbamic acid trichloromethyl ester(859807-24-2)
• EPA Substance Registry System: (4-nitro-phenyl)-carbamic acid trichloromethyl ester(859807-24-2)

Safety Data

• Hazardous Substances Data: 859807-24-2(Hazardous Substances Data)

Upstream product

• 32315-10-9 bis(trichloromethyl) carbonate 
• 100-01-6 4-nitro-aniline 
• 503-38-8 trichloromethyl chloroformate 

Downstream Products

• 57709-67-8 1-(4-nitrophenyl)-3-(2-amino-phenyl)urea 
• 1345415-26-0 C₃₂H₂₅N₅O₄ 
• 587-90-6 bis-N,N'-(4-nitrophenyl)urea 
• 75-44-5 phosgene 
• 100-28-7 4-Nitrophenyl isocyanate 
• 104-04-1 N-(4-Nitrophenyl)acetamide 

Relevant articles and documents

Triphenylamine-based simple chemosensor for selective fluorometric detection of fluoride, acetate and dihydrogenphosphate ions in different solvents

Triphenylamine-based new chemosensors 1 and 2 have been designed and synthesized for fluorometric detection of anions. The urea-amide conjugates in 1 and 2 are involved in binding of anions via hydrogen bonding. UV-vis and fluorescence titration experimen

Nucleophilic Substitutions at Carbonic Acid Derivatives. XX. Aminolysis of Bis(trichlormethyl)carbonate

The rate constants for the two steps of the reaction of bis(trichlormethyl)carbonate with substituted anilines have been determinated by conductivity measurements.The first relatively fast step of the reaction is the nucleophilic attack of the amine to the bis(trichloromethyl)carbonate leading to trichloromethylurethane through a six or four centers transition state in wich the carbon-nitrogen bond is formed parallel with the transfer of the proton.In this reaction a phosgene molecule is also produced, which reacts very fast with amine to form a N,N'-diarylurea.The s econd, much slower step, is the nucleophilic attack of the amine to the trichloromethylurethane.Through a similar transition state in which the proton transfer has even a higher importance, a N,N'-disubstituted urea and an other molecule of phosgene are formed.