113602-60-1

Basic information

• Product Name: Thiophene, 3-[(4-methoxyphenyl)thio]-
• CAS NO: 113602-60-1
• Molecular Formula: C11H10OS2
• Molecular Weight: 222.332
• Mol File: 113602-60-1.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Thiophene, 3-[(4-methoxyphenyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Thiophene, 3-[(4-methoxyphenyl)thio]-(113602-60-1)
• EPA Substance Registry System: Thiophene, 3-[(4-methoxyphenyl)thio]-(113602-60-1)

Safety Data

• Hazardous Substances Data: 113602-60-1(Hazardous Substances Data)

Upstream product

• 6165-69-1 Thien-3-ylboronic acid 
• 80472-59-9 S-(4-methoxyphenyl) (4-methylbenzene)thiosulfonate 
• 696-63-9 4-Methoxybenzenethiol 
• 5335-87-5 4,4'-dimethoxyphenyl disulfide 
• 88-13-1 3-Thiophene carboxylic acid 
• 10486-61-0 3-thienyl iodide 
• 872-31-1 3-Bromothiophene 
• 1317-39-1 copper(I) oxide 

Downstream Products

• 143509-69-7 4-<<3-<(N-isobutyl-N-methylamino)methyl>-4-hydroxyphenyl>sulfonyl>thiophene-2-sulfonamide 
• 143509-67-5 4-<<3-<(diethylamino)methyl>-4-hydroxyphenyl>sulfonyl>thiophene-2-sulfonamide 
• 128348-45-8 4-<<3-<(dimethylamino)methyl>-4-hydroxyphenyl>sulfonyl>thiophene-2-sulfonamide 
• 128348-28-7 4-(4-Methoxyphenylsulfonyl)thiophene-2-sulfonyl Chloride 
• 119731-18-9 4-(4-Methoxyphenylsulfonyl)thiophene-2-sulfonamide 
• 128348-42-5 4-(4-Hydroxyphenylsulfonyl)thiophene-2-sulfonamide 
• 128348-25-4 3-(4-Methoxyphenylsulfonyl)thiophene 

Relevant articles and documents

Forging C?S(Se) Bonds by Nickel-catalyzed Decarbonylation of Carboxylic Acid and Cleavage of Aryl Dichalcogenides

A nickel-catalyzed decarbonylation of carboxylic acids cross-coupling protocol has been developed for the straightforward C?S(Se) bond formation. This reaction is promoted by a commercially-available, user-friendly, inexpensive, air and moisture-stable nickel precatalyst. Various carboxylic acids and a wide range of aryl dichalcogenide substrates were tolerated in this process which afforded products in good to excellent yields. In addition, the present reaction can be conducted on gram scale in good yield.

Rhodium-catalyzed odorless synthesis of diaryl sulfides from borylarenes and: S -aryl thiosulfonates

Various diaryl sulfides, including heteroaryl- and nitrogen-containing sulfides, have been efficiently prepared by rhodium-catalyzed odorless deborylative arylthiolation of organoborons with S-aryl thiosulfonates. The ready availability of starting materials and further transformation of sulfides have rendered a diverse range of organosulfur compounds easily accessible.

N-1H-Tetrazol-5-yl-(5-Ring)-carboxamide-derivatives, a process for their manufacture, and the use thereof

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