1094348-31-8

Basic information

• Product Name: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one
• Synonyms: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one
• CAS NO: 1094348-31-8
• Molecular Weight: 246.33
• Mol File: 1094348-31-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one(1094348-31-8)
• EPA Substance Registry System: 3-(4-methoxyphenyl)-1-(thiophen-2-yl)propan-1-one(1094348-31-8)

Safety Data

• Hazardous Substances Data: 1094348-31-8(Hazardous Substances Data)

Upstream product

• 696-62-8 para-iodoanisole 
• 393148-57-7 1-thiophen-2-yl-prop-2-en-1-ol 
• 6028-93-9 (2E)-3-(4-methoxyphenyl)-1-(thiophen-2-yl) prop-2-en-1-one 
• 40570-64-7 3-chloro-1-(2-thienyl)propan-1-one 
• 5720-07-0 4-methoxyphenylboronic acid 

Downstream Products

• 2810-04-0 Ethyl thiophene-2-carboxylate 
• 221915-87-3 1,1,1-trifluoro-4-(4-methoxy-phenyl)-butan-2-one 

Relevant articles and documents

Fabrication of Pd/CuFe2O4 hybrid nanowires: A heterogeneous catalyst for Heck couplings

The development of environmentally benign transformations is indispensable in organic synthesis. Herein, a hybrid heterogeneous catalyst, palladium(0) on copper ferrite nanowires, has been synthesized, characterized, and for the first time, employed in the Jeffrey Heck reaction between iodoarenes and allylic alcohols, and good to excellent yields have been obtained. In addition, the catalyst was found to be suitable for the usual Heck coupling. The nanocatalyst was recovered and reused up-to multiple runs without any noticeable loss of its catalytic activity.

Rhodium(I)-catalyzed arylation of β-chloro ketones and related derivatives through domino dehydrochlorination/conjugate addition

Highly efficient arylations of β-chloro ketones and their ester and amide derivatives were achieved by means of domino dehydrochlorination/Rh(I)- catalyzed conjugate addition. In situ generated vinyl ketones and their analogues were identified as the reaction intermediates. The present synthetic protocol provides a concise route to (chiral) β-aryl ketones, esters, and amides. Copyright