346663-54-5

Basic information

• Product Name: N-(4-methylphenyl)-2-(2-thienyl)acetamide
• Synonyms: N-(4-methylphenyl)-2-(2-thienyl)acetamide
• CAS NO: 346663-54-5
• Molecular Formula: C13H13NOS
• Molecular Weight: 231.31342
• Mol File: 346663-54-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-(4-methylphenyl)-2-(2-thienyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methylphenyl)-2-(2-thienyl)acetamide(346663-54-5)
• EPA Substance Registry System: N-(4-methylphenyl)-2-(2-thienyl)acetamide(346663-54-5)

Safety Data

• Hazardous Substances Data: 346663-54-5(Hazardous Substances Data)

Upstream product

• 39098-97-0 2-thienylacetic acid chloride 
• 106-49-0 p-toluidine 
• 4461-29-4 2-(thiophen-2-yl)acetamide 
• 29540-83-8 p-tolyl triflate 
• 99-99-0 1-methyl-4-nitrobenzene 
• 13939-06-5 molybdenum hexacarbonyl 

Relevant articles and documents

Palladium Catalyzed Aminocarbonylation of Benzylic Ammonium Triflates with Nitroarenes: Synthesis of Phenylacetamides

A palladium catalyzed reductive aminocarbonylation of benzylic ammonium triflates with nitroarenes for the synthesis of phenylacetamides was developed. Using Pd(acac)2/DPPF catalyst system, a range of different substituted phenylacetamides were prepared in moderate to good yields from benzylic ammonium triflates and nitroarenes through Csp3?N bond cleavage. A variety of alkyl, aryl, and halide substituents on both substrates can be used, and many useful functional groups can be tolerated. (Figure presented.).

Synthesis and biological evaluation of N-(aryl)-2-thiophen-2-ylacetamides series as a new class of antitubercular agents

The present article describes a series of 21 N-(aryl)-2-thiophen-2-ylacetamides, which were synthesized and evaluated for their in vitro antibacterial activity against Mycobacterium tuberculosis, and the activity expressed as the minimum inhibitory concen