317335-12-9

Usage

Uses

Used in Pharmaceutical Applications:
1-(5-benzylthiophen-2-yl)ethanone is used as an enzyme inhibitor for its potential role in the development of pharmaceuticals. Its ability to inhibit specific enzymes makes it a candidate for therapeutic applications, particularly in the treatment of various diseases where enzyme inhibition is a desired outcome.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(5-benzylthiophen-2-yl)ethanone is used as a key intermediate in the synthesis of a range of organic compounds. Its unique structure allows for the creation of diverse molecules with potential applications in various industries.
Used in Materials Science:
1-(5-benzylthiophen-2-yl)ethanone is also being investigated for its potential applications in materials science. Its properties may contribute to the development of new materials with specific characteristics, such as improved conductivity or enhanced stability.

Upstream product

• 100-39-0 benzyl bromide 
• 206551-43-1 (5-acetylthiophen-2-yl)boronic acid 
• 100-44-7 benzyl chloride 
• 88-15-3 2-Acetylthiophene 
• 13132-15-5 2-benzylthiophene 
• 108-24-7 acetic anhydride 
• 61464-23-1 (5-bromothiophen-2-yl)(phenyl)methanol 
• 100-52-7 benzaldehyde 
• 5370-25-2 2-Acetyl-5-bromothiophene 
• 78191-00-1 N-Methoxy-N-methylacetamide 
• 117175-13-0 2-benzyl-5-bromothiophene 

Downstream Products

• 102655-56-1 1-(5-benzyl-[2]thienyl)-5,9-dimethyl-deca-2,4,8-trien-1-one 
• 13132-16-6 5-benzylthiophene-2-carboxylic acid 
• 1430823-37-2 C₁₃H₁₀O₂S 
• 1430823-41-8 5-(5-benzylthiophen-2-yl)pyrazine-2,3-dicarbonitrile 
• 102655-57-2 (+/-)-1-(5-benzyl-[2]thienyl)-3ξ-(2,6,6-trimethyl-cyclohex-2-enyl)-propenone 
• 5581-75-9 6-phenylhexanic acid 

Relevant academic research and scientific papers

Photo-Ni-Dual-Catalytic C(sp2)-C(sp3) Cross-Coupling Reactions with Mesoporous Graphitic Carbon Nitride as a Heterogeneous Organic Semiconductor Photocatalyst

The synergistic combination of a heterogeneous organic semiconductor mesoporous graphitic carbon nitride (mpg-CN) and a homogeneous nickel catalyst with visible-light irradiation at room temperature affords the C(sp2)-C(sp3) cross-co

Thiophen-2-yl and bithienyl substituted pyrazine-2,3-dicarbonitriles as precursors for tetrasubstituted zinc azaphthalocyanines

Peripheral thiophen-2-yl substituents extend the macrocyclic conjugation of zinc(II)azaphthalocyanines, (ZnAzaPc), due to coplanarity between the two ring systems, and red-shifted UV-Vis Q-bands are observed. This lowering in energy is favourable for vari

Suzuki-miyaura cross-couplings mediated by trans-PdBr(N-Succ)(PPh 3)2: A convenient synthetic method for diarylmethanes and aryl(heteroaryl)- methanes

Diarylmethanes can be accessed efficiently by Suzuki-Miyaura cross-couplings of arylboronic acids with benzyl halides mediated by trans-PdBr(N-Succ) (PPh3)2. The methodology can be applied to the synthesis of aryl(heteroaryl)methanes. Georg Thieme Verlag Stuttgart New York.

Palladium-catalyzed benzylation of heterocyclic aromatic compounds

Broadly applicable palladium-catalyzed heteroarene benzylation reactions are described with a focus on the most challenging heterocyclic classes under traditional benzylation techniques such as sulfur-containing heterocycles and those bearing functional groups that would be incompatible with reactions requiring Lewis acids and/or strong bases.

Simple palladium(II) precatalyst for suzuki-miyaura couplings: Efficient reactions of benzylic, aryl, heteroaryl, and vinyl coupling partners

trans-PdBr(N-Succ)(PPh3)2 (1) is a universally effective precatalyst for Suzuki-Miyaura cross-couplings of benzylic halides with aryl- or heteroarylboronic acids. Substituted aryl halides and halogenated cyclic enones can be cross-coupled with aryl- or vinylboronic acids in excellent yields. Catalyst recycling is also demonstrated.

1-(Aromatic- or heteroaromatic-substituted)-3-(heteroaromatic substituted)-1,3-propanediones and uses thereof

Certain 1-(aromatic- or heteroaromatic-substituted-3-(heteroaromatic substituted)-1,3-propanediones are described as inhibitors of HIV integrase and inhibitors of HIV replication. These compounds are useful in the prevention or treatment of infection by HIV and the treatment of AIDS, either as compounds, pharmaceutically acceptable salts, pharmaceutical composition ingredients, whether or not in combination with other antivirals, immunomodulators, antibiotics or vaccines. Methods of treating AIDS and methods of preventing or treating infection by HIV are also described.