154191-77-2

Basic information

• Product Name: methyl 2-(2-(thiophen-2-yl)phenyl)acetate
• Synonyms: methyl 2-(2-(thiophen-2-yl)phenyl)acetate
• CAS NO: 154191-77-2
• Molecular Weight: 232.303
• Mol File: 154191-77-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 2-(2-(thiophen-2-yl)phenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(2-(thiophen-2-yl)phenyl)acetate(154191-77-2)
• EPA Substance Registry System: methyl 2-(2-(thiophen-2-yl)phenyl)acetate(154191-77-2)

Safety Data

• Hazardous Substances Data: 154191-77-2(Hazardous Substances Data)

Upstream product

• 6165-68-0 thiophene boronic acid 
• 57486-69-8 methyl 2-(2-bromophenyl)acetate 
• 18698-97-0 ortho-bromophenylacetic acid 
• 6072-49-7 2-(2'-carboxyphenyl)thiophene 
• 97677-81-1 2-(2'-chloroformylphenyl)thiophene 
• 1003-09-4 2-bromothiophene 
• 956229-86-0 methyl 2-(2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetate 
• 67-56-1 methanol 
• 106183-47-5 α-diazo-2-(2-thienyl)acetophenone 

Downstream Products

• 958219-45-9 2-[2-(2-thienyl)phenyl]acetic acid 
• 154191-76-1 methyl diazo<2-(3,4,5-trichloro-2-thienyl)phenyl>acetate 
• 154191-78-3 methyl <2-(3,4,5,-trichloro-2-thienyl)phenyl>acetate 

Relevant articles and documents

Identification of two novel thiophene analogues as inducers of autophagy mediated cell death in breast cancer cells

Natural compounds isolated from different medicinal plants remain one of the major resources of anticancer drugs due to their enormous chemical diversity. Studies suggested therapeutic potential for various tanshinones, key bioactive lipophilic compounds

Potentially Aromatic Thiophenium Ylides. V. Reactions of Ethoxycarbonyl- (and Methoxycarbonyl)-2-(2-thienyl)phenylcarbene

In an attempt to make thiophenium ylides in which the ylide bond is part of a five-membered ring annulated to the α-side of the thiophene moiety, two alkoxycarbonyl substituted 2-(2-thienyl)phenylcarbenes have been made, with and without chlorine substituents in the remaining thiophene positions.With rhodium acetate as a catalyst the carbene without chlorines cyclized to the 3-position of the thiophene to give a fluorene analogue, whereas no cyclization was detected when the 3-position was blocked.