10220-98-1

Basic information

• Product Name: Benzenecarbothioamide, N-cyclohexyl-
• CAS NO: 10220-98-1
• Molecular Formula: C13H17NS
• Molecular Weight: 219.351
• Mol File: 10220-98-1.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzenecarbothioamide, N-cyclohexyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarbothioamide, N-cyclohexyl-(10220-98-1)
• EPA Substance Registry System: Benzenecarbothioamide, N-cyclohexyl-(10220-98-1)

Safety Data

• Hazardous Substances Data: 10220-98-1(Hazardous Substances Data)

Upstream product

• 150-60-7 dibenzyl disulphide 
• 108-91-8 cyclohexylamine 
• 103-82-2 phenylacetic acid 
• 108-88-3 toluene 
• 110-91-8 morpholine 
• 141-84-4 2-thioxo-4-thiazolidinone 
• 1759-68-8 N-benzoylcyclohexylamine 
• 100-52-7 benzaldehyde 
• 98-07-7 Benzotrichlorid 
• 128204-63-7 N-benzoyl-S-thiobenzoylsulfenamide 
• 3682-36-8 dithiobenzoic acid sodium salt 
• 35124-71-1 S-(Thiobenzoyl)-hydrosulfamin 
• 121-68-6 dithiobenzoic acid 
• 611-73-4 Benzoylformic acid 

Downstream Products

• 1759-68-8 N-benzoylcyclohexylamine 
• 100616-90-8 1-cyclohexyl-5-phenyl-1H-tetrazole 
• 113327-11-0 1-((2R,5S)-3-Cyclohexyl-2-ethoxy-4-oxo-2,5-diphenyl-thiazolidin-5-yl)-4-phenyl-[1,2,4]triazolidine-3,5-dione 
• 113327-04-1 C₂₇H₃₃N₃O₆S 
• 113327-03-0 C₂₆H₃₁N₃O₆S 
• 83927-22-4 N-Cyclohexyl-thiobenzimidic acid phenyl ester 
• 882-33-7 diphenyldisulfane 
• 113326-84-4 3-cyclohexyl-2,5-diphenylthiazolium-4-olate 

Relevant articles and documents

Sulfonic acid functionalized nano Γ-Al 2O 3: A new, efficient, and reusable catalyst for synthesis of thioamides

Sulfonic acid functionalized nano γ-Al2O3 is easily prepared by the reaction of nano γ-Al2O3 with 1,3-propane sulfone. This reagent can be used as an eficient catalyst for the synthesis of thioamides. This new method consistently has the advantages of excellent yields and short reaction times. Further, the catalyst can be recovered for several times.

Sulfur-Catalyzed Oxidative Coupling of Dibenzyl Disulfides with Amines: Access to Thioamides and Aza Heterocycles

In the presence of catalytic amounts of elemental sulfur, dibenzyl disulfide/DMSO was found to be an excellent thiobenzoylating agent of amines to provide a wide range of thioamides. The reaction becomes autocatalytic when anilines substituted by an o-cyclizable group were used as nucleophile, leading to the corresponding 2-aryl aza heterocycles. (Figure presented.).

Decarboxylative thioamidation of arylacetic and cinnamic acids: A new approach to thioamides

A new decarboxylative strategy has been developed for the synthesis of thioamides via a three-component reaction involving arylacetic or cinnamic acids, amines and elemental sulfur powder, without the need of a transition metal and an external oxidant.