40231-24-1

Basic information

• Product Name: Carbamodithioic acid, phenyl-
• Synonyms: Phenyl-dithiocarbamidsaeure;Dithiocarbanilsaeure;N-Phenyl-dithiocarbamidsaeure;phenyl-dithiocarbamic acid;N-phenyldithiocarbamic acid
• CAS NO: 40231-24-1
• Molecular Formula: C7H7NS2
• Molecular Weight: 169.271
• Mol File: 40231-24-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Carbamodithioic acid, phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamodithioic acid, phenyl-(40231-24-1)
• EPA Substance Registry System: Carbamodithioic acid, phenyl-(40231-24-1)

Safety Data

• Hazardous Substances Data: 40231-24-1(Hazardous Substances Data)

Upstream product

• 75-15-0 carbon disulfide 
• 62-53-3 aniline 

Downstream Products

• 96424-04-3 Phenyl-dithiocarbamic acid N'-[5-(5,6,7,8-tetrahydro-naphthalen-2-yl)-[1,2,4]triazin-3-yl]-hydrazinocarbonylmethyl ester 
• 103-72-0 phenyl isothiocyanate 
• 1457-46-1 3-phenylrhodanine 
• 81411-30-5 6,8-dimethyl-2,4-dithia-6,8-diaza-7,9-dioxo-3-phenyliminobicyclo<3.2.2>nonane 
• 144809-98-3 Phenyl-dithiocarbamic acid (R)-((R)-5-oxo-2-phenyl-4,5-dihydro-oxazol-4-yl)-phenyl-methyl ester 
• 144809-89-2 N-((5R,6R)-4-Oxo-3,6-diphenyl-2-thioxo-[1,3]thiazinan-5-yl)-benzamide 
• 149-30-4 2-thioxo-3H-1,3-benzothiazole 
• 1843-21-6 N-phenyl-2-benzothiazolamine 
• 7783-06-4 hydrogen sulfide 
• 102-08-9 N,N-diphenylthiourea 
• 5351-69-9 4-Phenyl-3-thiosemicarbazide 
• 1282612-15-0 C₃₉H₅₂N₆O₂S₂ 
• 1346544-92-0 C₃₂H₄₅N₃O₃S 
• 1313419-76-9 C₉H₈NO₂S₂^(1-)*Na⁽¹⁺⁾ 

Relevant articles and documents

Microwave-assisted synthesis and antibacterial activity of novel chenodeoxycholic acid thiosemicarbazone derivatives

A rapid and efficient method for the synthesis of novel chenodeoxycholic acid thiosemicarbazone derivatives under solvent-free conditions using microwave irradiation is reported. Ten novel compounds have been synthesised in good yields. Their structures were elucidated by 1H NMR, IR, ESI-MS spectra and elemental analysis. Preliminary results showed that some of these compounds possess inhibitory effects against S. typhimurium and E. coli.

Cobalt mediated by desulfurization toward the synthesis of isothiocyanates

A highly efficient and simple protocol for the construction of aromatic and aliphatic isothiocyanates from their respective amines in the presence of cheap, readily available, and air-stable cobalt catalyst is described. All reactions were carried out under optimized reaction conditions and gave target products in good to excellent yields within shorter reaction time.

Synthesis of new hyodeoxycholic acid thiosemicarbazone derivatives under solvent-free conditions using microwave

An efficient and simple method for synthesis of new hyodeoxycholic acid thiosemicarbazone derivatives under solvent-free conditions using microwave has been developed. Its main advantages are short reaction times, good conversions and the environmentally friendly nature of the process. The preliminary results indicate that some of these compounds possess inhibitory effects against E. coli.