13456-63-8

Basic information

• Product Name: benzaldehyde N-phenylthiosemicarbazone
• CAS NO: 13456-63-8
• Molecular Formula: C₁₄H₁₃N₃S
• Molecular Weight: 255.3381
• Mol File: 13456-63-8.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 390.9°C at 760 mmHg
• Flash Point: 190.2°C
• Density: 1.14g/cm³
• Vapor Pressure: 2.56E-06mmHg at 25°C
• Refractive Index: 1.618
• CAS DataBase Reference: benzaldehyde N-phenylthiosemicarbazone(CAS DataBase Reference)
• NIST Chemistry Reference: benzaldehyde N-phenylthiosemicarbazone(13456-63-8)
• EPA Substance Registry System: benzaldehyde N-phenylthiosemicarbazone(13456-63-8)

Safety Data

• Hazardous Substances Data: 13456-63-8(Hazardous Substances Data)

Usage

General Description

Benzaldehyde N-phenylthiosemicarbazone is a chemical compound formed from benzaldehyde and N-phenylthiosemicarbazide. It is a yellow crystalline solid that is commonly used in organic synthesis and as a reagent in analytical chemistry. It is known for its inhibitory properties against the corrosion of mild steel and for its antifungal and antibacterial activities. Additionally, benzaldehyde N-phenylthiosemicarbazone has been studied for its potential use in the treatment of various diseases and disorders, including cancer and diabetes. It is a versatile compound with a range of potential applications in both laboratory and industrial settings.

Upstream product

• 100-52-7 benzaldehyde 
• 5351-69-9 4-Phenyl-3-thiosemicarbazide 
• 7664-41-7 ammonia 
• 103-72-0 phenyl isothiocyanate 
• 302-01-2 hydrazine 
• 79-19-6 thiosemicarbazide 
• 108-94-1 cyclohexanone 
• 34025-58-6 2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9-one 
• 62-53-3 aniline 
• 51034-34-5 potassium aniline dithiocarbamate 
• 101569-98-6 Cinnamoylameisensaeure-<4-phenyl-thiosemicarbazon> 
• 28867-76-7 benzaldehyde benzylidenehydrazone 
• 5281-18-5 benzaldehyde, hydrazone 
• 64-17-5 ethanol 

Downstream Products

• 98177-16-3 benzaldehyde (5-methyl-4-oxo-3-phenyl-thiazolidin-2-ylidene)-hydrazone 
• 1093399-52-0 4-amino-1-benzoyl-2,7-dinitro-4'-phenylspiro(fluoren-9,3'-[1,2,4]triazolidine)-5'-thione 
• 1437-57-6 phenyl-(5-phenyl-3H-[1,3,4]thiadiazol-2-ylidene)amine 
• 84409-01-8 4-amino-2,7-dinitro-9-fluorenone 
• 1093399-46-2 (1-benzoyl-4-phenyl-3-thioxo-1,2,4-triazaspiro[4.5]deca-6,9-dien-8-ylidene)malononitrile 
• 1093399-40-6 4a-hydroxy-3-phenylindeno[2,1-e][1,3,4]oxadiazin-9(4aH)-one 
• 1093399-45-1 3-cyano-4-oxo-N-phenylideno[1,2-c]pyrazole-1(4H)-carbothioamide 
• 1092341-31-5 C₂₄H₂₀N₄OS 
• 1174624-69-1 ethyl 3-amino-6-phenyl-5-cyanopyridazine-4-carboxylate 
• 1174624-63-5 ethyl [3-phenyl-4-oxo-1-(phenylthiocarbamoyl)-4,5-dihydro-1H-pyrazol-5-ylidene]cyanoacetate 
• 1174624-57-7 methyl [3-phenyl-4-oxo-1-(phenylthiocarbamoyl)-4,5-dihydro-1H-pyrazol-5-ylidene]ethanoate 
• 1415313-62-0 trans-[Ni(κ2-N3, S-C14H12N3S)2] 

Relevant articles and documents

A new "switch-On" fluorescence chemosensor for anions via modulation of intraligand and metal-to-ligand charge-transfer emission in a Pd(II)-based receptor

A new mechanism for anion sensing by fluorescence spectroscopy based on modulation of intraligand fluorescence (IL) and metal-to-ligand charge-transfer (MLCT) emission from a weakly fluorescent metal complex was investigated. Elemental analysis of the rec

Phenyl -2 - shrinkage N4 -Phenyl thiosemicarbazone aryl ruthenium complex as well as preparation method and application thereof

The invention discloses a phenyl-2-acetal N-phenyl thiosemicarbazide ruthenium aryl complex as well as a preparation method and application thereof. The complex has a structural formula (III) in the specification. The chemical name of the complex is trichloromonomethyl isopropylbenzene ruthenium (II) monochloro-phenyl-2-acetal N-phenyl thiosemicarbazide-methyl isopropylbenzene ruthenium (II). The complex shows good inhibitory activities towards gastric cancer SGC7901 cell lines and liver cancer BEL-7404 cell lines, can be used for preparing medicines for treating cancers, and can be used after being prepared into the forms, such as injections, tablets, pills, capsules, suspending agents or emulsion. The preparation method of the phenyl-2-acetal N-phenyl thiosemicarbazide ruthenium aryl complex is simple, is accessible in raw materials and has the advantage of low cost.

Synthesis and biological evaluation of novel benzoquinones as potential antimicrobial agents

New series of 2,5-dihydroxyphenyl-1,3-thiazoles 4a-l was synthesized by reacting 2,5-dihydroxyphenacyl bromide with various 4-aryl thiosemicarbazones 3a-l that on oxidation with ferric chloride yielded the corresponding N 1-substituted benzylid