82020-27-7

Basic information

• Product Name: 4-methoxy-N-(4-methoxyphenyl)benzenecarbothioamide
• CAS NO: 82020-27-7
• Molecular Formula: C₁₅H₁₅NO₂S
• Molecular Weight: 273.3501
• Mol File: 82020-27-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 403.7°C at 760 mmHg
• Flash Point: 197.9°C
• Density: 1.219g/cm³
• Vapor Pressure: 1E-06mmHg at 25°C
• Refractive Index: 1.646
• CAS DataBase Reference: 4-methoxy-N-(4-methoxyphenyl)benzenecarbothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-N-(4-methoxyphenyl)benzenecarbothioamide(82020-27-7)
• EPA Substance Registry System: 4-methoxy-N-(4-methoxyphenyl)benzenecarbothioamide(82020-27-7)

Safety Data

• Hazardous Substances Data: 82020-27-7(Hazardous Substances Data)

Upstream product

• 100-66-3 methoxybenzene 
• 2284-20-0 4-Methoxyphenyl isothiocyanate 
• 27865-44-7 4-methoxy-N-(4-methoxyphenyl)benzamide 
• 104-94-9 4-methoxy-aniline 
• 100-07-2 4-methoxy-benzoyl chloride 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 101971-78-2 Acetic acid 4-[3-(4-acetoxy-phenyl)-5-ethyl-[1,2,4]triazol-4-yl]-phenyl ester 
• 82020-07-3 bis (methoxy-4 phenyl)-3,4 ethyl-5 4H-triazole-1,2,4 
• 82020-39-1 4,4'-(3-ethyl-4H-1,2,4-triazol-4,5-diyl)-bis-phenol 
• 94847-70-8 methoxy-4 N-(methoxy-4 phenyl) benzamide hydrazone 
• 53876-72-5 bis (methoxy-4 phenyl)-3,6 dihydro-1,2 tetrazine-1,2,4,5 
• 10205-70-6 6-methoxy-2-(4-methoxyphenyl)benzo[d]thiazole 

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.

Synthesis of thioamides by catalyst-free three-component reactions in water

Three-component reactions involving amines, aldehydes, and elemental sulfur powder are reported to afford thioamides in a simple one-pot procedure in the absence of a catalyst. A variety of thioamides can be obtained in good to excellent yields up to 88 %. Three-component reactions involving amines, aldehydes, and sulfur powder afford thioamides in a simple one-pot procedure. A variety of substituted thioamides are obtained in good to excellent yields up to 88 %. Copyright

Efficient synthesis of thiobenzanilides by Willgerodt-Kindler reaction with base catalysts

Willgerodt-Kindler reaction between anilines and benzaldehydes readily proceeded in the presence of catalytic amount of Na2S·9H 2O to give thiobenzanilides in moderate to good yields. The base catalyst was also available for preparation of primary thiobenzamide. Georg Thieme Verlag Stuttgart.