572922-96-4 Usage
Description
(S)-4-METHYL-3-(4-TRIFLUOROMETHYLPHENYL)OXAZOLIDIN-2-ONE is a chiral chemical compound belonging to the oxazolidinone class. It is characterized by its specific three-dimensional arrangement of atoms, which may contribute to its potential biological activity. The presence of trifluoromethyl and methyl groups in its structure influences its chemical and biological properties, making it a compound of interest for further study in pharmaceuticals and other fields.
Uses
Used in Pharmaceutical Industry:
(S)-4-METHYL-3-(4-TRIFLUOROMETHYLPHENYL)OXAZOLIDIN-2-ONE is used as a potential pharmaceutical compound for its unique structure and chirality. Its trifluoromethyl and methyl groups may contribute to its biological activity, making it a candidate for drug development and other applications in the pharmaceutical field.
Used in Drug Development:
(S)-4-METHYL-3-(4-TRIFLUOROMETHYLPHENYL)OXAZOLIDIN-2-ONE is used as a compound of interest in drug development due to its potential biological activity. Further study of this compound could provide insight into its possible uses in creating new medications and therapies.
Used in Research and Development:
(S)-4-METHYL-3-(4-TRIFLUOROMETHYLPHENYL)OXAZOLIDIN-2-ONE is used as a subject of research and development in various scientific fields. Its unique structure and properties make it a valuable compound for exploring new applications and understanding its potential impact on pharmaceuticals and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 572922-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,2,9,2 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 572922-96:
(8*5)+(7*7)+(6*2)+(5*9)+(4*2)+(3*2)+(2*9)+(1*6)=184
184 % 10 = 4
So 572922-96-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10F3NO2/c1-7-6-17-10(16)15(7)9-4-2-8(3-5-9)11(12,13)14/h2-5,7H,6H2,1H3/t7-/m0/s1
572922-96-4Relevant articles and documents
Influence of the catalyst structure in the cycloaddition of isocyanates to oxiranes promoted by tetraarylstibonium cations
Yang, Mengxi,Pati, Nilanjana,Bélanger-Chabot, Guillaume,Hirai, Masato,Gabba?, Fran?ois P.
supporting information, p. 11843 - 11850 (2018/09/10)
In the context of our work on electron deficient group 15 cations as Lewis acid catalysts, we have synthesized the triflate salts of a series of tetraarylstibonium cations of general formula [ArSbPh3]+ with Ar = Mes (4+), o-(dimethylamino)phenyl (5+), and o-((dimethylamino)methyl)phenyl (6+). These new cationic antimony derivatives, along with the known [Ph4Sb]+ (1+), 1-naphthyltriphenylstibonium (2+), and [(Ant)SbPh3]+ (3+), have been evaluated as catalysts for the cycloaddition of oxiranes and isocyanates under mild conditions. While all stibonium cations favor the 3,4-oxazolidinone products, the reactivities of 5+ and 6+ are hindered by the ancillary amino donor which quenches the Lewis acidity of the antimony center. A comparison of the other stibonium cations shows that 4+ is the most selective catalyst.
Iodine(V) reagents in organic synthesis. Part 3. New routes to heterocyclic compounds via o-iodoxybenzoic acid-mediated cyclizations: Generality, scope, and mechanism
Nicolaou,Baran,Zhong,Barluenga,Hunt,Kranich,Vega
, p. 2233 - 2244 (2007/10/03)
The discovery and development of the o-iodoxybenzoic acid (IBX) reaction with certain unsaturated N-aryl amides (anilides) to form heterocycles are described. The application of the method to the synthesis of δ-lactams, cyclic urethanes, hydroxy amines, and amino sugars among other important building blocks and intermediates is detailed. In addition to the generality and scope of this cyclization reaction, this article describes a number of mechanistic investigations suggesting a single electron transfer from the anilide functionality to IBX and implicating a radical-based mechanism for the reaction.
