19982-41-3

Basic information

• Product Name: N'-(2-ethoxy-benzoyl)-hydrazinecarbodithioic acid; potassium salt
• Synonyms: N'-(2-ethoxy-benzoyl)-hydrazinecarbodithioic acid; potassium salt
• CAS NO: 19982-41-3
• Molecular Weight: 294.44
• Mol File: 19982-41-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N'-(2-ethoxy-benzoyl)-hydrazinecarbodithioic acid; potassium salt(CAS DataBase Reference)
• NIST Chemistry Reference: N'-(2-ethoxy-benzoyl)-hydrazinecarbodithioic acid; potassium salt(19982-41-3)
• EPA Substance Registry System: N'-(2-ethoxy-benzoyl)-hydrazinecarbodithioic acid; potassium salt(19982-41-3)

Safety Data

• Hazardous Substances Data: 19982-41-3(Hazardous Substances Data)

Upstream product

• 3686-55-3 methyl 2-ethoxybenzoate 
• 134-11-2 2-ethoxybenzoic acid 
• 6290-24-0 ethyl 2-ethoxybenzoate 
• 75-15-0 carbon disulfide 
• 21018-13-3 2-ethoxybenzoic acid hydrazide 

Downstream Products

• 851879-31-7 4-amino-5-(2-ethoxy-phenyl)-2,4-dihydro-[1,2,4]triazole-3-thione 
• 19982-34-4 5-(2-ethoxy-phenyl)-3H-[1,3,4]oxadiazol-2-one 
• 19982-27-5 5-[5-(2-ethoxy-phenyl)-[1,3,4]oxadiazol-2-ylsulfanylmethyl]-3H-[1,3,4]oxadiazol-2-one 
• 19982-31-1 3-acetyl-5-(2-ethoxy-phenyl)-3H-[1,3,4]oxadiazol-2-one 
• 19982-36-6 2-(2,4-dinitro-phenylsulfanyl)-5-(2-ethoxy-phenyl)-[1,3,4]oxadiazole 
• 19982-33-3 2-ethanesulfonyl-5-(2-ethoxy-phenyl)-[1,3,4]oxadiazole 
• 19982-37-7 2-(2-ethoxy-phenyl)-5-ethylsulfanyl-[1,3,4]oxadiazole 
• 19982-30-0 [5-(2-ethoxy-phenyl)-[1,3,4]oxadiazol-2-ylsulfanyl]-acetic acid ethyl ester 
• 19982-28-6 [5-(2-ethoxy-phenyl)-[1,3,4]oxadiazol-2-ylsulfanyl]-acetic acid hydrazide 
• 19982-29-7 [5-(2-ethoxy-phenyl)-[1,3,4]oxadiazol-2-ylsulfanyl]-acetic acid 
• 19982-39-9 5-(2-ethoxy-phenyl)-3H-[1,3,4]thiadiazole-2-thione 
• 19982-38-8 2-(o.etossifenil)-5-mercapto-1,3,4-oxadiazolo 

Relevant articles and documents

Ultrasound-assisted, one-pot, three-component synthesis and antibacterial activities of novel indole derivatives containing 1,3,4-oxadiazole and 1,2,4-triazole moieties

Thirteen novel indole derivatives were efficiently synthesized through ultrasound irradiation by using 4-amino-5-(1H-indol-3-yl)-4H-[1,2,4]triazole-3-thiol (8) and 2-mercapto-5-substituted-1,3,4-oxadiazoles (5a-m). Compared with conventional and microwave methods, yields increased to 82-93%, and reaction times decreased to 15-35 min. The structures of these novel compounds were characterized by spectral data and elemental analysis. Two out of the synthesized compounds (10f and 10l) exhibited excellent activity against Staphylococcus aureus and Escherichia coli, and thus warrant further research.

Identification of a potent new chemotype for the selective inhibition of PDE4

A series of substituted 3,6-diphenyl-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazines were prepared and analyzed as inhibitors of phosphodiesterase 4 (PDE4). Synthesis, structure-activity relationships, and the selectivity of a highly potent analogue against related phosphodiesterase isoforms are presented.