175203-54-0 Usage
Description
1-[5-(2-PHENYLETH-1-YNYL)-2-THIENYL]ETHAN-1-ONE is a chemical compound belonging to the ketone class of organic compounds, characterized by a molecular formula of C16H12OS. It features a thienyl and phenylethynyl group, which contribute to its unique structure and potential reactivity. 1-[5-(2-PHENYLETH-1-YNYL)-2-THIENYL]ETHAN-1-ONE is mainly utilized in research and scientific studies, particularly within the realms of organic chemistry and drug development.
Uses
Used in Organic Chemistry Research:
1-[5-(2-PHENYLETH-1-YNYL)-2-THIENYL]ETHAN-1-ONE is used as a research compound for exploring its chemical properties and potential reactivity in organic chemistry. Its unique structure allows scientists to investigate its behavior in various chemical reactions and interactions.
Used in Drug Development:
In the pharmaceutical and medicinal chemistry industries, 1-[5-(2-PHENYLETH-1-YNYL)-2-THIENYL]ETHAN-1-ONE is used as a potential candidate for drug development. Its distinctive molecular structure may offer new avenues for the creation of novel therapeutic agents, although further research is required to fully understand its potential applications and optimize its use in this field.
Additional research is necessary to delve deeper into the properties and potential applications of 1-[5-(2-PHENYLETH-1-YNYL)-2-THIENYL]ETHAN-1-ONE, ensuring that its full potential can be harnessed across various scientific and industrial domains.
Check Digit Verification of cas no
The CAS Registry Mumber 175203-54-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,2,0 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 175203-54:
(8*1)+(7*7)+(6*5)+(5*2)+(4*0)+(3*3)+(2*5)+(1*4)=120
120 % 10 = 0
So 175203-54-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H10OS/c1-11(15)14-10-9-13(16-14)8-7-12-5-3-2-4-6-12/h2-6,9-10H,1H3
175203-54-0Relevant articles and documents
Alkynylboranes: A practical approach by zinc-catalyzed dehydrogenative coupling of terminal alkynes with 1,8-naphthalenediaminatoborane
Tsuchimoto, Teruhisa,Utsugi, Hirokazu,Sugiura, Tetsuya,Horio, Shin
, p. 77 - 82 (2015/02/19)
Under zinc Lewis acid catalysis, terminal alkynes coupled dehydrogenatively with 1,8-naphthalenediaminatoborane [HB(dan)]. It is important to note that the resulting alkynylboranes with an C(sp) - B(dan) bond are isolable by column chromatography on silica gel (SiO2) and are usable as coupling partners for palladium- and copper-catalyzed cross-coupling reactions with (hetero)aryl halides.
Mild Pd/Cu-catalyzed sila-sonogashira coupling of (hetero)aryl bromides with (hetero)arylethynylsilanes under PTC conditions
Bellina, Fabio,Lessi, Marco
experimental part, p. 773 - 777 (2012/07/01)
The palladium/copper cocatalyzed sila-Sonogashira reaction of (hetero)arylethynysilanes with (hetero)aryl bromides in toluene and water at 40 C under PTC conditions gave the required di(hetero)arylethynes in moderate to high yields. Activated, deactivated and ortho-substituted (hetero)aryl bromides are well tolerated. This protocol also allowed the preparation of symmetrical diarylethynes by double arylation of 1,2-bis(trimethylsilyl)ethyne. Georg Thieme Verlag Stuttgart · New York.
Palladhim-catalyzed decarboxylative sp-sp2 cross-coupling reactions of aryl and vinyl halides and triflates with α,β-ynoic acids using silver oxide
Kim, Hyunseok,Lee, Phil Ho
scheme or table, p. 2827 - 2832 (2010/03/26)
Palladium-catalyzed decarboxylative sp-sp2 cross-coupling reactions of aryl and vinyl halides and triflates with α,β-ynoic acids using silver oxide have been developed. A variety of α,β-ynoic acids were readily decarboxylated in the presence of
