24786-18-3

Basic information

• Product Name: dimethyl N-benzoyldithiocarbonimidate
• Synonyms: dimethyl N-benzoyldithiocarbonimidate
• CAS NO: 24786-18-3
• Molecular Weight: 225.335
• Mol File: 24786-18-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: dimethyl N-benzoyldithiocarbonimidate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl N-benzoyldithiocarbonimidate(24786-18-3)
• EPA Substance Registry System: dimethyl N-benzoyldithiocarbonimidate(24786-18-3)

Safety Data

• Hazardous Substances Data: 24786-18-3(Hazardous Substances Data)

Upstream product

• 75-15-0 carbon disulfide 
• 55-21-0 benzamide 
• 74-88-4 methyl iodide 
• 98-91-9 thiobenzoic acid 
• 77-78-1 dimethyl sulfate 
• 21406-30-4 N-Benzoylamino-dithiokohlensaeuremethylester 
• 74-93-1 methylthiol 
• 333-20-0 potassium thioacyanate 
• 98-88-4 benzoyl chloride 

Downstream Products

• 13996-86-6 N-(Benzoyl)thiocarbamidsaeure-S-methylester 
• 25508-17-2 S-methyl-N-benzoylisothiourea 
• 73999-12-9 N-benzoyl-S-methyl-N'-phenyl-isothiourea 
• 88735-95-9 N-((Z)-2-Cyano-1-methylsulfanyl-3-oxo-3-phenyl-propenyl)-benzamide 
• 74074-25-2 1-Benzoyl-3-(4-methoxy-phenyl)-2-methyl-isothiourea 
• 61903-35-3 4-ethoxy-6-phenyl-[1,3,5]triazin-2-ylamine 
• 14945-93-8 4-methylsulfanyl-6-phenyl-[1,3,5]-triazin-2-ylamine 
• 16192-17-9 N-(3,4,5,6-tetrahydro-1H-pyrimidin-2-ylidene)benzamide 
• 16192-18-0 N-(4,5,6,7-tetrahydro-1H-[1,3]diazepin-2-yl)-benzamide 
• 7412-05-7 N-(1H-benzo[d]imidazol-2-yl)benzamide 
• 5005-14-1 N-(benzo[d]thiazol-2-yl)benzamide 
• 74074-26-3 1-Benzoyl-3-(4-bromo-phenyl)-2-methyl-isothiourea 
• 88735-88-0 N-(2,2-Dicyano-1-(methylthio)vinyl)benzamide 
• 118996-48-8 methyl (Z)-3-benzamido-2-cyano-3-methylthiopropenoate 

Relevant articles and documents

Synthesis of benzoxazole amides as novel antifungal agents against Malassezia furfur

Malassezia is a pathogenic fungus that causes skin diseases, such as tinea versicolor, atopic dermatitis and fatal sepsis. We report the synthesis of a series of benzoxazole amides and evaluation of their antifungal activity against Malassezia furfur. Twe

An α-hydrazinoalkylphosphonate as building block for novel N-phosphonoalkylheterocycles

α-Hydrazinoalkylphosphonate 3 is a useful building block for the syntheses of novel N-phosphonoalkylheterocycles. N-phosphonoalkylpyrazoles 8 and 9 were prepared by the cyclization reaction of 3 with malfunctioned ethenes 5 and 6 in ethanol under reflux. N-Phosphonoalkyltriazole 10 was synthesized from 3 with N-dimethylthiomethylene benzoyl amide 4 in ethanol under reflux. The structures were confirmed by IR, 1H NMR, mass spectroscopy, and elemental analysis. At the same time, the preparation of 4 was investigated.

Reactions with N-Acylimino-dithiocarbonic-acid-diesters

Reactions of N-acylimino-dithiocarbonic-acid-S,S-diesters 1 with nucleophilic compounds present new possibilities to synthesize heterocycles.With amines 1a reacts by mono- and disubstitution, respectively, of methylthio-groups to isothioureas 2 and guanidines 3, with 1,2-binucleophilic arenes to benzoheterocycles 4, with aliphatic diamines to imidazolines 5, pyrimidines 6, diazepines 7 and the hexamethylene-diamine-derivatives 8. 1a reacts also with hydrazines to 1,2,4-triazoles 9 and with hydrazides to the thiosemicarbazones 10 or 1,3,4-oxadiazoles 11.Heterocyclisations of 1 with guanidines, thiourea, salts of thiourea and amidines give the 1,3,5-triazines 12, 14, 15 and 16.N-benzoyl-dithiocarbonic-acid-methylester -amid reacts with CH-acidic compounds to thiazoles 17.The structures of the final products are determined by i.r.-, 1H-n.m.r.-, u.v.- and mass-spectras.