26060-23-1

Basic information

• Product Name: 4-methoxy-N-phenylbenzenecarbothioamide
• Synonyms: 4-methoxy-N-phenylbenzenecarbothioamide
• CAS NO: 26060-23-1
• Molecular Formula: C₁₄H₁₃NOS
• Molecular Weight: 243.32412
• Mol File: 26060-23-1.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 367.3°Cat760mmHg
• Flash Point: 176°C
• Appearance: /
• Density: 1.215g/cm³
• CAS DataBase Reference: 4-methoxy-N-phenylbenzenecarbothioamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-N-phenylbenzenecarbothioamide(26060-23-1)
• EPA Substance Registry System: 4-methoxy-N-phenylbenzenecarbothioamide(26060-23-1)

Safety Data

• Hazardous Substances Data: 26060-23-1(Hazardous Substances Data)

Upstream product

• 4270-58-0 4-hydroxy-N-phenylbenzothioamide 
• 77-78-1 dimethyl sulfate 
• 34009-55-7 2-(4-methoxy-phenyl)-3-phenyl-5-thioxo-4,5-dihydro-[1,3,4]thiadiazolium betaine 
• 133218-27-6 N-(4-Methoxy-thiobenzoyl)-3,N-diphenyl-propionamide 
• 7465-88-5 4-methoxy-N-phenylbenzamide 
• 7446-70-0 aluminium trichloride 
• 103-72-0 phenyl isothiocyanate 
• 100-66-3 methoxybenzene 
• 123-11-5 4-methoxy-benzaldehyde 
• 62-53-3 aniline 
• 782-45-6 4-amino-benzoic acid anilide 
• 3460-11-5 4-nitrobenzanilide 
• 3054-31-7 4-amino-thiobenzoic acid anilide 
• 104-01-8 4-Methoxyphenylacetic acid 

Downstream Products

• 6265-92-5 2-(4-methoxy-phenyl)-benzothiazole 
• 61522-27-8 5-ethoxycarbonyl-2-(4-methoxy-phenyl)-4-oxo-3-phenyl-4,5-dihydro-thiazolium betaine 
• 61522-26-7 2-(4-methoxy-phenyl)-4-oxo-3,5-diphenyl-4,5-dihydro-thiazolium betaine 
• 133218-27-6 N-(4-Methoxy-thiobenzoyl)-3,N-diphenyl-propionamide 
• 3333-52-6 2,2,3,3-tetramethylsuccinonitrile 
• 7465-88-5 4-methoxy-N-phenylbenzamide 
• 57761-70-3 5-(4-methoxyphenyl)-1-phenyl-1H- tetrazole 

Relevant articles and documents

Visible-Light Carbon Nitride-Catalyzed Aerobic Cyclization of Thiobenzanilides under Ambient Air Conditions

A metal-free heterogeneous photocatalysis has been developed for the synthesis of benzothiazoles via intramolecular C-H functionalization/C-S bond formation of thiobenzanilides by inexpensive graphitic carbon nitride (g-C3N4) under visible-light irradiation. This reaction provides access to a broad range of 2-substituted benzothiazoles in high yields under an air atmosphere at room temperature without addition of a strong base or organic oxidizing reagents. In addition, the catalyst was found to be stable and reusable after five reaction cycles.

Functionalization of activated methylene C-H bonds with nitroarenes and sulfur for the synthesis of thioamides

We report a method to obtain arylthioamides by the functionalization of sp3 C-H bonds in phenylacetic acids and benzyl alcohols. Reactions proceeded without the use of any solvents and were compatible with many functionalities and heterocycles. These conditions allow for a rapid synthesis of thioamides from simple, commercial substrates.

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.