116114-18-2

Basic information

• Product Name: Benzoic acid, 4-chloro-, 2-[(ethylamino)carbonyl]hydrazide
• CAS NO: 116114-18-2
• Molecular Formula: C10H12ClN3O2
• Molecular Weight: 241.677
• Mol File: 116114-18-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-chloro-, 2-[(ethylamino)carbonyl]hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-chloro-, 2-[(ethylamino)carbonyl]hydrazide(116114-18-2)
• EPA Substance Registry System: Benzoic acid, 4-chloro-, 2-[(ethylamino)carbonyl]hydrazide(116114-18-2)

Safety Data

• Hazardous Substances Data: 116114-18-2(Hazardous Substances Data)

Upstream product

• 536-40-3 4-chlorobenzoic acid hydrazide 
• 109-90-0 ethyl isocyanate 

Downstream Products

• 117258-18-1 5-(4-Chloro-phenyl)-4-ethyl-2-propyl-2,4-dihydro-[1,2,4]triazol-3-one 
• 31409-32-2 5-(4-Chlorophenyl)-4-ethyl-2,4-dihydro-3H-1,2,4-triazol-3-one 
• 110623-26-2 5-(4-Chlorophenyl)-4-ethyl-2-methyl-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 116114-14-8 5-(4-Chlorophenyl)-2,4-dihydro-4-ethyl-2-methyl-3H-1,2,4-triazol-3-one 

Relevant articles and documents

The rapid preparation of 2-aminosulfonamide-1,3,4-oxadiazoles using polymer-supported reagents and microwave heating

Herein, we report on the preparation of a library of 5-substituted-2-amino- 1,3,4-oxadiazoles and the corresponding thiadiazole analogues. Presented is a one-pot preparation of the 2-aminosulfonylated analogues through a three component coupling of an acylhydrazine, an isocyanate and sulfonyl chloride promoted by a polymer-supported phosphazine base under microwave dielectric heating. Also described is the optimization process and details pertaining to the elucidation of the reaction products.

5-phenyl-3H-1,2,4-triazol-3-ones and their use as anticonvulsants

This invention relates to 5-phenyl-3H-1,2,4-triazol-3-ones and to their use as anticonvulsants for treatment of seizure disorders.

Process for the preparation of 5-aryl-2,4-dialkyl-3H-1,2,4-triazole-3-thiones

This invention relates to a novel process for the preparation of 5-aryl-2,4-dialkyl-3H-1,2,4-triazole-3--thiones, useful as antidepressants, through the thionation of the corresponding 5-aryl-2,4-dialkyl-3H-1,2,4-triazol--3-ones.