19182-34-4

Basic information

• Product Name: (4-fluorophenyl)carbamodithioic acid
• CAS NO: 19182-34-4
• Molecular Formula: C₇H₆FNS₂*H₃N
• Molecular Weight: 187.2576
• Mol File: 19182-34-4.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 246.7°C at 760 mmHg
• Flash Point: 103°C
• Density: 1.417g/cm³
• Vapor Pressure: 0.0267mmHg at 25°C
• Refractive Index: 1.699
• CAS DataBase Reference: (4-fluorophenyl)carbamodithioic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4-fluorophenyl)carbamodithioic acid(19182-34-4)
• EPA Substance Registry System: (4-fluorophenyl)carbamodithioic acid(19182-34-4)

Safety Data

• Hazardous Substances Data: 19182-34-4(Hazardous Substances Data)

Usage

General Description

(4-fluorophenyl)carbamodithioic acid is a chemical compound with the formula C7H6FNS2. It is a derivative of carbamodithioic acid, containing a 4-fluorophenyl group. (4-fluorophenyl)carbamodithioic acid is used in the synthesis of pharmaceuticals and agrochemicals, and it is also employed as a reagent in organic chemistry. It is known for its potential biological activities and has been studied for its potential use in various therapeutic applications. Additionally, it is important to handle this compound with caution, as it may pose health risks if not handled properly.

Upstream product

• 75-15-0 carbon disulfide 
• 371-40-4 4-fluoroaniline 

Downstream Products

• 1309469-85-9 4-[(10S)-dihydroartemisinin-10-oxy]benzaldehyde N₄-(4-fluorophenyl)thiosemicarbazone 
• 330-94-9 4-(4-fluorophenyl)thiosemicarbazide 
• 199111-93-8 4-(4-fluorophenyl)-5-(pyridin-2-yl)-4H-1,2,4-triazole-3-thiol 
• 199111-94-9 4-(4'-fluorophenyl)-5-(pyridin-4'-yl)-4H-1,2,4-triazole-3-thiol 
• 636-12-4 N-(4'-fluorophenyl)-2-isonicotinoylhydrazine-1-carbothioamide 
• 1544-68-9 4-fluorophenyl isothiocyanate 
• 117682-43-6 (4-Fluoro-phenyl)-dithiocarbamic acid 4-oxo-2,3-diphenyl-thiazolidin-5-yl ester 
• 1547-15-5 3‐(4‐fluorophenyl)‐2‐thioxo‐2,3‐dihydroquinazolin‐4(1H)‐one 
• 117664-62-7 (4-Fluoro-phenyl)-dithiocarbamic acid 3-(3-chloro-phenyl)-4-oxo-2-phenyl-thiazolidin-5-yl ester 
• 117664-61-6 (4-Fluoro-phenyl)-dithiocarbamic acid 3-(4-chloro-phenyl)-4-oxo-2-phenyl-thiazolidin-5-yl ester 

Relevant articles and documents

Synthesis and antimicrobial activity of some new 1,2,4-trizoles

A series of 1,2,4-triazole derivatives were synthesized using appropriate synthetic route and structures were confirmed by IR,1H NMR and elemental analysis. All the synthesized compounds (6a-6h and 7a-7h) were evaluated for antimicrobial activity by determining their minimum inhibitory concentrations (MICs) against a panel of Gram-positive, Gram-negative bacteria and fungi. Most of the compounds showed significant antimicrobial activity against Gram-positive bacteria viz. S. aureus, B. subtilis, Gram-negative bacteria viz. E. coli, P. aerugenosa and fungi viz. C. albicans, A. niger. Some of the compounds showed better antibacterial activities against Gram-positive bacteria compared to Gram-negative bacteria. Compounds 7g, 6g, 6a exhibited good MICs against Gram-positive bacteria and 7f showed better MICs against Gram-negative bacteria compared to reference norfloxacin. Compounds 7f and 7d exhibited MICs which is equipotent to the reference drug ketoconazole.