2613-12-9

Basic information

• Product Name: benzaldehyde N-methylthiosemicarbazone
• CAS NO: 2613-12-9
• Molecular Formula: C₉H₁₁N₃S
• Molecular Weight: 193.2687
• Mol File: 2613-12-9.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 297°C at 760 mmHg
• Flash Point: 133.4°C
• Density: 1.13g/cm³
• Vapor Pressure: 0.00138mmHg at 25°C
• Refractive Index: 1.591
• CAS DataBase Reference: benzaldehyde N-methylthiosemicarbazone(CAS DataBase Reference)
• NIST Chemistry Reference: benzaldehyde N-methylthiosemicarbazone(2613-12-9)
• EPA Substance Registry System: benzaldehyde N-methylthiosemicarbazone(2613-12-9)

Safety Data

• Hazardous Substances Data: 2613-12-9(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 6610-29-3 4-methylthiosemicarbazide 

Downstream Products

• 53884-77-8 benzylidene-(3,4-dimethyl-3H-thiazol-2-ylidene)-hydrazine 
• 67399-18-2 2-(benzylidenehydrazinylidene)-2,3-dihydro-3-methyl-4-phenyl-1,3-thiazole 
• 1415313-61-9 trans-[Ni(κ2-N3, S-C9H10N3S)2] 
• 1173295-27-6 C₁₉H₁₈N₄OS 
• 96984-81-5 2-benzylidenehydrazino-3-methyl-1,3-thiazolidin-4-one 
• 72926-10-4 4-Acetyl-2-(acetylmethylamino)-5-phenyl-Δ²-1,3,4-thiadiazoline 
• 38942-51-7 4-methyl-3-phenyl-1H-1,2,4-triazole-5(4H)-thione 
• 3161-81-7 2-benzylidenehydrazono-3,4-dimethyl-2,3-dihydro-thiazole-5-carboxylic acid ethyl ester 
• 3161-72-6 2-(benzylidene-methyl-hydrazino)-4-methyl-thiazole-5-carboxylic acid ethyl ester 
• 27434-47-5 1-benzyl-4-methyl-thiosemicarbazide 
• 14537-64-5 methyl-(5-phenyl-[1,3,4]thiadiazol-2-yl)-amine 

Relevant articles and documents

The influence of benzaldehyde-N-alkyl-thiosemicarbazones on the synthesis of gold(I) ionic complexes: Spectroscopy, ESI-mass, structures and variable H-bonded polymeric networks

The effect of the substituents at the N1/C2 atoms of the thiosemicarbazones R1R2C2 = N3-N2H-C1(=S)-N1HR3 on the type of gold(I) complexes is inve

Inhibitions of monoamine oxidases and acetylcholinesterase by 1-methyl, 5-phenyl substituted thiosemicarbazones: Synthesis, biochemical, and computational investigations

A series of eleven 1-methyl, 5-phenyl substituted thiosemicarbazones (MT1–MT11) with the phenyl ring substitutions were prepared and investigated for their inhibitory activities against monoamine oxidases (MAOs) and acetylcholinesterase (AChE). [4-(dimeth