62774-59-8

Basic information

• Product Name: Hydrazinecarboxamide, N-(4-methoxyphenyl)-
• Synonyms: 4-(4'-methoxyphenyl)-3-semicarbazide;4-(4-Methoxy-phenyl)-semicarbazid;4-(4-methoxyphenyl)semicarbazide;Hydrazinecarboxamide,N-(4-methoxyphenyl);N-p-Anisyl-semicarbazid;N-(4-methoxyphenyl)hydrazinecarboxamide;4-(p-Anisyl)semicarbazid;(4-methoxyphenyl)semicarbazide
• CAS NO: 62774-59-8
• Molecular Formula: C8H11N3O2
• Molecular Weight: 181.194
• Mol File: 62774-59-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Hydrazinecarboxamide, N-(4-methoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarboxamide, N-(4-methoxyphenyl)-(62774-59-8)
• EPA Substance Registry System: Hydrazinecarboxamide, N-(4-methoxyphenyl)-(62774-59-8)

Safety Data

• Hazardous Substances Data: 62774-59-8(Hazardous Substances Data)

Upstream product

• 537-80-4 2,2,2-trifluoroethyl-N-4-methoxyphenylcarbamate 
• 2040-77-9 4-methoxyphenylcarbamic chloride 
• 104-94-9 4-methoxy-aniline 
• 20950-96-3 (4-methoxyphenyl)carbamic acid phenyl ester 
• 1566-42-3 p-anisidine urea 
• 917-61-3 sodium isocyanate 
• 5416-93-3 4-Methoxyphenyl isocyanate 
• 110-20-3 acetone semicarbazone 

Downstream Products

• 1198272-57-9 1-(2-ethyl-4-oxo-4H-quinazolin-3-yl)-3-(4-methoxy-phenyl)-urea 
• 80240-44-4 (4-methoxyphenyl)triazolone 
• 1155338-52-5 C₁₆H₁₄N₄O₃ 
• 1287216-28-7 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde 4-(4-methoxyphenyl)semicarbazone 
• 1357066-60-4 4-[(5-[4-methoxylphenylamino]-1,3,4-oxadiazol-2-yl)methylamino]-1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one 
• 1155338-52-5 N-(4-methoxyphenyl)-2-(2-oxoindolin-3-ylidene)hydrazine-1-carboxamide 

Relevant articles and documents

Synthesis, In-vitro evaluation and molecular docking studies of oxoindolin phenylhydrazine carboxamides as potent and selective inhibitors of ectonucleoside triphosphate diphosphohydrolase (NTPDase)

Members of the ectonucleoside triphosphate diphosphohydrolases (NTPDases) constitute the major family of enzymes responsible for the maintenance of extracellular levels of nucleotides and nucleosides by catalyzing the hydrolysis of nucleoside triphosphate

Synthesis, cytotoxicity, and in vivo antitumor activity study of parthenolide semicarbazones and thiosemicarbazones

Parthenolide is an important sesquiterpene lactone with potent anticancer activities. In order to further improve its biological activity, a series of parthenolide semicarbazone or thiosemicarbazone derivatives was synthesized and evaluated for their anti

Highly Regioselective Carbamoylation of Electron-Deficient Nitrogen Heteroarenes with Hydrazinecarboxamides

The use of hydrazinecarboxamides as a new class of carbamoylating agents has been established through the dehydrazinative Minisci reaction of electron-deficient nitrogen heteroarenes. A wide range of electron-deficient nitrogen heteroarenes, including isoquinoline, quinoline, pyridine, phenanthridine, quinoxaline, and phthalazine, underwent copper/acid-catalyzed oxidative carbamoylation with hydrazinecarboxamide hydrochlorides to afford structurally diverse nitrogen-heteroaryl carboxamides as single regioisomers in moderate to excellent yields. The functional group tolerance was substantially demonstrated in the direct carbamoylation of quinine obviating multistep sequences involving protecting groups and prefunctionalization of the heterocycle.