317335-12-9 Usage
Description
1-(5-benzylthiophen-2-yl)ethanone, with the molecular formula C15H14OS, is a chemical compound that exists as a yellowish liquid with a strong odor. It is widely utilized in the synthesis of various organic compounds and is recognized for its potential biological activities, such as inhibiting certain enzymes. Due to its potential hazards if mishandled, caution is advised during its use. Ongoing research aims to explore its possible applications in fields like pharmaceuticals and materials science.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 317335-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,3 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 317335-12:
(8*3)+(7*1)+(6*7)+(5*3)+(4*3)+(3*5)+(2*1)+(1*2)=119
119 % 10 = 9
So 317335-12-9 is a valid CAS Registry Number.
317335-12-9Relevant articles and documents
Photo-Ni-Dual-Catalytic C(sp2)-C(sp3) Cross-Coupling Reactions with Mesoporous Graphitic Carbon Nitride as a Heterogeneous Organic Semiconductor Photocatalyst
Antonietti, Markus,Ghosh, Indrajit,K?nig, Burkhard,Khamrai, Jagadish,Savateev, Aleksandr
, p. 3526 - 3532 (2020/04/09)
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
Palladium-catalyzed benzylation of heterocyclic aromatic compounds
Lapointe, David,Fagnou, Keith
supporting information; experimental part, p. 4160 - 4163 (2009/12/07)
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
Burns, Michael J.,Fairlamb, Ian J. S.,Kapdi, Anant R.,Sehnal, Petr,Taylor, Richard J. K.
, p. 5397 - 5400 (2008/09/17)
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.
