27421-65-4

Basic information

• Product Name: Hydrazinecarbothioamide, N-methyl-2-(1-phenylethylidene)-
• CAS NO: 27421-65-4
• Molecular Formula: C10H13N3S
• Molecular Weight: 207.299
• Mol File: 27421-65-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Hydrazinecarbothioamide, N-methyl-2-(1-phenylethylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Hydrazinecarbothioamide, N-methyl-2-(1-phenylethylidene)-(27421-65-4)
• EPA Substance Registry System: Hydrazinecarbothioamide, N-methyl-2-(1-phenylethylidene)-(27421-65-4)

Safety Data

• Hazardous Substances Data: 27421-65-4(Hazardous Substances Data)

Upstream product

• 6610-29-3 4-methylthiosemicarbazide 
• 98-86-2 acetophenone 
• 52756-49-7 C₉H₈N₂S 
• 74-89-5 methylamine 
• 13466-30-3 (1-phenylethylidene)hydrazine 

Downstream Products

• 1357348-61-8 Pd(κ3-C4,N3,S-acetophenone-N-methylthiosemicarbazonato) 
• 27422-17-9 methyl-[5-oxo-4-(1-phenyl-ethyl)-4,5-dihydro-[1,3,4]thiadiazol-2-yl]-carbamoyl chloride 
• 26365-37-7 trimethyl-[5-oxo-4-(1-phenyl-ethyl)-4,5-dihydro-[1,3,4]thiadiazol-2-yl]-urea 
• 26365-36-6 1,3-dimethyl-1-[5-oxo-4-(1-phenyl-ethyl)-4,5-dihydro-[1,3,4]thiadiazol-2-yl]-urea 
• 27434-48-6 4-methyl-1-(1-phenyl-ethyl)-thiosemicarbazide 

Relevant articles and documents

Organometallic ruthenium(II) complexes containing NS donor Schiff bases: Synthesis, structure, electrochemistry, DNA/BSA binding, DNA cleavage, radical scavenging and antibacterial activities

Four new cyclopentadienylruthenium(II)-acetophenone-4(N)-substituted thiosemi-carbazone complexes, with the general formula [Ru(?5-C5H5)(H-Aptsc)PPh3].Cl (1), [Ru(?5-C5H5)(H-Apmt

M-STAGE KINESIN INHIBITOR

A mitotic kinesin Eg5 inhibitor which comprises a thiadiazoline derivative represented by the general formula (I) or a pharmacologically acceptable salt thereof as an active ingredient: [wherein R1 represents a hydrogen atom and the like, R2 represents a hydrogen atom, -C(=W)R6 (wherein W represents an oxygen atom or a sulfur atom, and R6 represents substituted or unsubstituted lower alkyl and the like) and the like, R3 represents -C(=Z)R19 (wherein Z represents an oxygen atom or a sulfur atom, and R19 represents substituted or unsubstituted lower alkyl and the like) and the like, R4 represents substituted or unsubstituted lower alkyl and the like, and R5 represents substituted or unsubstituted aryl and the like] and the like are provided.