21406-30-4

Basic information

• Product Name: Carbamodithioic acid, benzoyl-, methyl ester
• CAS NO: 21406-30-4
• Molecular Formula: C9H9NOS2
• Molecular Weight: 211.309
• Mol File: 21406-30-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Carbamodithioic acid, benzoyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamodithioic acid, benzoyl-, methyl ester(21406-30-4)
• EPA Substance Registry System: Carbamodithioic acid, benzoyl-, methyl ester(21406-30-4)

Safety Data

• Hazardous Substances Data: 21406-30-4(Hazardous Substances Data)

Upstream product

• 98-91-9 thiobenzoic acid 
• 556-64-9 methyl thiocyanate 
• 75-15-0 carbon disulfide 
• 55-21-0 benzamide 
• 77-78-1 dimethyl sulfate 
• 74-93-1 methylthiol 
• 333-20-0 potassium thioacyanate 
• 98-88-4 benzoyl chloride 
• 16696-83-6 S-methyl dithiocarbamate 
• 98-91-9 thiobenzoic acid 

Downstream Products

• 108676-88-6 N-(N-benzoylthiocarbamoyl-glycyl)-glycine 
• 123965-45-7 N-benzoylthiocarbamoyl-phenylalanine p-toluidide 
• 114538-66-8 N-benzoylthiocarbamoyl-norleucine p-toluidide 
• 7245-61-6 N-[(benzoylamino)thioxomethyl]glycine 
• 7139-34-6 5-phenyl-3(3H)-thioxo-1,2,4-dithiazole 
• 71389-25-8 2,2-bis-methylsulfanyl-4-phenyl-2H-[1,3]oxazete 
• 74074-51-4 (2-Methylsulfanyl-4-phenyl-thiazol-5-yl)-phenyl-methanone 
• 14598-05-1 3-methylsulfanyl-5-phenyl-[1,2,4]dithiazolylium; iodide 
• 7047-10-1 5-phenyl-3H-1,2,4-dithiazole-3-one 
• 24786-21-8 3-methylsulfanyl-5-phenyl-[1,2,4]oxadiazole 
• 73999-12-9 N-benzoyl-S-methyl-N'-phenyl-isothiourea 
• 25508-17-2 S-methyl-N-benzoylisothiourea 
• 116055-58-4 N-(4-methyl-5-oxo-4,5-dihydro-thiazol-2-yl)-benzamide; hydrochloride 
• 61903-35-3 4-ethoxy-6-phenyl-[1,3,5]triazin-2-ylamine 

Relevant articles and documents

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.