1202680-24-7

Basic information

• Product Name: phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate
• Synonyms: phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate
• CAS NO: 1202680-24-7
• Molecular Weight: 285.086
• Mol File: 1202680-24-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate(1202680-24-7)
• EPA Substance Registry System: phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate(1202680-24-7)

Safety Data

• Hazardous Substances Data: 1202680-24-7(Hazardous Substances Data)

Usage

General Description

Phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate is a chemical compound that belongs to the pyridazine family. It is characterized by a phenyl group attached to a pyridazine ring, with two chlorine atoms located at the 4th and 5th positions. The compound also contains a carboxylate group at the 1st position of the pyridazine ring. This chemical exhibits potential biological activity and can be used in various fields, such as pharmaceuticals, agrochemicals, and materials science. Further research is needed to explore its specific properties and applications in different industries.

Upstream product

• 932-22-9 4,5-dichloro-2H-pyridazin-3-one 
• 1885-14-9 phenyl chloroformate 

Downstream Products

• 16641-71-7 1-(phenoxycarbonyl)piperidine 
• 56379-88-5 cyclohexylcarbamic acid phenyl ester 
• 2387-23-7 1,3-Dicyclohexylurea 
• 621-00-1 1,3-di-p-tolylurea 
• 33275-26-2 N-(4-methylphenyl)-O-phenyl carbamate 
• 50882-28-5 phenyl N-(4-chlorophenyl)carbamate 
• 1219-99-4 N,N'-bis(4-chlorophenyl)urea 
• 1227-44-7 N,N'-bis(4-methoxyphenyl)urea 
• 20950-96-3 (4-methoxyphenyl)carbamic acid phenyl ester 
• 56379-81-8 O-phenyl N-(2-phenylethyl)carbamate 
• 5467-84-5 1,3-diphenethylurea 
• 3898-47-3 phenyl-N-butylcarbamate 
• 142075-48-7 phenyl N,N-diisopropylcarbamate 
• 4930-03-4 phenyl N-phenylcarbamate 

Relevant articles and documents

Phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate as carbonyl source: Facile and selective synthesis of carbamates and ureas under mild conditions

The selective syntheses of carbamates, symmetric -ureas, and unsymmetrical ureas have been accomplished by the -reaction of amines with phenyl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylate as a carbonyl source under mild conditions. It is noteworthy that this process is mild, economic, and convenient.

Synthesis of organic carbonates with alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates and ROH/AlCl3under ambient condition

We demonstrated the synthesis of organic carbonates using alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates and alcohol in the presence of aluminum chloride. Alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates were reacted with alcohol in the presence of AlCl3 in toluene at room temperature to afford the corresponding unsymmetric and symmetric organic carbonates in good to excellent yields. These are efficient and convenient processes. Alkyl/aryl 4,5-dichloro-6-oxopyridazine-1(6H)-carboxylates are solid, stable and non-toxic CO2/CO2R(Ar) source. It is noteworthy that the reaction is carry out under an ambient and acidic conditions, the easy-to prepare and readily available starting materials and the quantitative isolation of reusable 4,5-dichloropyridazin-3(2H)-one.