21076-11-9

Basic information

• Product Name: 4-(4-METHYLPHENYL)-3-THIOSEMICARBAZIDE
• Synonyms: N1-(4-METHYLPHENYL)HYDRAZINE-1-CARBOTHIOAMIDE;N-(4-METHYLPHENYL)HYDRAZINECARBOTHIOAMIDE;4-(4-METHYLPHENYL)-3-THIOSEMICARBAZIDE;4-METHYLPHENYLTHIOSEMICARBAZIDE;AKOS BBS-00000507;4-(4-Methylpheny-3-thisemicarbazide;3-aMino-1-(4-Methylphenyl)thiourea;3-amino-1-methyl-1-phenylthiourea
• CAS NO: 21076-11-9
• Molecular Formula: C₈H₁₁N₃S
• Molecular Weight: 181.26
• Mol File: 21076-11-9.mol
• Article Data: 13

Chemical Properties

• Melting Point: 135-136°C
• Boiling Point: 302.7 °C at 760 mmHg
• Flash Point: 136.8 °C
• Appearance: /
• Density: 1.27 g/cm³
• PKA: 11.07±0.70(Predicted)
• CAS DataBase Reference: 4-(4-METHYLPHENYL)-3-THIOSEMICARBAZIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-METHYLPHENYL)-3-THIOSEMICARBAZIDE(21076-11-9)
• EPA Substance Registry System: 4-(4-METHYLPHENYL)-3-THIOSEMICARBAZIDE(21076-11-9)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 21076-11-9(Hazardous Substances Data)

Usage

General Description

4-(4-methylphenyl)-3-thiosemicarbazide is a chemical compound with the molecular formula C9H11N3S. It is an organic compound that belongs to the class of thiosemicarbazides. 4-(4-METHYLPHENYL)-3-THIOSEMICARBAZIDE is commonly used in the synthesis of various heterocycles and organic compounds due to its ability to form stable complexes with metal ions. It is also used in the field of medicinal chemistry for the development of potential drug candidates. Additionally, 4-(4-methylphenyl)-3-thiosemicarbazide may have potential applications in agriculture as a pesticide or fungicide due to its biological activity. Overall, this compound has various uses and potential applications in different fields due to its unique chemical properties.

Upstream product

• 37600-51-4 methyl-phenyl-dithiocarbamic acid 
• 100-61-8 N-methylaniline 
• 75-15-0 carbon disulfide 
• 20069-27-6 2-(N-Phenyl-N-methyl-thiocarbamoylthio)acetic Acid 
• 55246-66-7 Imidazole-1-carbothioic acid methyl-phenyl-amide 

Downstream Products

• 135765-63-8 C₁₇H₁₉N₅S₂ 
• 847867-85-0 di-2-pyridyl ketone N⁽⁴⁾-methyl, N⁽⁴⁾-phenylthiosemicarbazone 
• 6499-14-5 pyrrolidine-1-carbothioic acid hydrazide 
• 100-61-8 N-methylaniline 
• 21198-50-5 piperidine-1-carbothioic acid hydrazide 
• 6499-15-6 4-morpholinothiosemicarbazide 
• 41197-43-7 thiomorpholine-4-carbothiohydrazide 
• 6507-37-5 azepane-1-carbothioic acid hydrazide 
• 87555-65-5 N'-(6,7-dihydroquinolin-8(5H)-ylidene)-4-(pyridine-2-yl)piperazine-1-carbothiohydrazide 
• 88324-31-6 1-methyl-1-phenyl-6-<1-(2-pyridinyl-ethylidene)amino>-2,5-dithiobiurea 
• 2112-92-7 methyl-phenyl-[1,3,4]thiadiazol-2-yl-amine 
• 34551-25-2 methyl-phenyl-[1,2,3,4]thiatriazol-5-yl-amine 
• 51984-13-5 C₁₂H₁₁N₅S 

Relevant articles and documents

Synthesis, Crystal Structure, and In Vitro Cytotoxic, Antitumor And Antimicrobial Evaluation of a New Pyrazole Derivative N-3,5-Trimethyl-Nphenyl-1-H-Pyrazole-1-Carbothioamide

Anew pyrazole molecule of N-3,5-trimethyl-N-phenyl-1-H-pyrazole-1-carbothioamide (MePhPyC) has been synthesized and characterized by elemental analysis, single crystal x-ray diffraction (XRD), and mass, 1H NMR, ultraviolet-visible (UV-Vis), and

Synthesis, characterization and biological studies of cobalt(II), nickel(II), copper(II) and zinc(II) complexes of vanillin-4-methyl-4-phenyl-3-thiosemicarbazone

Abstract: Complexes of vanillin-4-methyl-4-phenyl-3-thiosemicarbazone with cobalt(II), nickel((II), copper(II) and zinc(II) metal ions were synthesized and characterized by elemental analysis, molar conductance, magnetic moment, infrared spectra, electron

Imaging intracellular zinc by using a glyoxal bis(4-methyl-4-phenyl-3- thiosemicarbazone) ligand

The ligand glyoxal bis(4-methyl-4-phenyl-3-thiosemicarbazone) (GTSCH 2) is shown to be a selective fluorescence "turn-on" sensor for zinc ions (Zn2+). This sensor is easy to synthesize, exhibits excellent sensitivity and selectivity