220628-99-9 Usage
Uses
Used in Pharmaceutical Industry:
(S)-4-PHENYL-2-(QUINOLIN-8-YL)-4,5-DIHYDROOXAZOLE is used as a potential drug candidate for the development of medications with anti-inflammatory properties, targeting conditions such as arthritis and other inflammatory diseases. Its anti-inflammatory action can help alleviate pain, swelling, and redness associated with these conditions.
Used in Oncology:
In the field of oncology, (S)-4-PHENYL-2-(QUINOLIN-8-YL)-4,5-DIHYDROOXAZOLE is used as a potential anti-tumor agent, contributing to the development of novel cancer treatments. Its anti-tumor properties may aid in inhibiting the growth and spread of cancer cells, offering a new therapeutic approach for various types of cancer.
Used in Microbiology:
(S)-4-PHENYL-2-(QUINOLIN-8-YL)-4,5-DIHYDROOXAZOLE is used as a potential anti-bacterial agent, with applications in the development of new antibiotics to combat bacterial infections. Its anti-bacterial properties can help in targeting and eliminating harmful bacteria, contributing to the treatment and prevention of various bacterial diseases.
Used in Organic Synthesis:
In the field of organic chemistry, (S)-4-PHENYL-2-(QUINOLIN-8-YL)-4,5-DIHYDROOXAZOLE serves as a valuable precursor for the preparation of other biologically active compounds. Its unique structure allows for further chemical modifications and the synthesis of new molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Research and Development:
(S)-4-PHENYL-2-(QUINOLIN-8-YL)-4,5-DIHYDROOXAZOLE is used as a subject of study in scientific research and development, where its properties and potential applications are explored. This includes investigating its pharmacological effects, optimizing its synthesis, and evaluating its safety and efficacy for various therapeutic uses.
Check Digit Verification of cas no
The CAS Registry Mumber 220628-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,6,2 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220628-99:
(8*2)+(7*2)+(6*0)+(5*6)+(4*2)+(3*8)+(2*9)+(1*9)=119
119 % 10 = 9
So 220628-99-9 is a valid CAS Registry Number.
220628-99-9Relevant academic research and scientific papers
Chiral pyridylmethyl- and quinolinyl-oxazolines as ligands for enantioselective palladium-catalyzed allylic alkylation
Chelucci, Giorgio,Gladiali, Serafino,Saba, Antonio
, p. 1393 - 1400 (2007/10/03)
Chiral pyridylmethyl- and quinolinyl-oxazolines were prepared and assessed in the enantioselective palladium-catalyzed allylic substitution of 1,3-diphenylprop-2-enyl acetate with dimethyl malonate. Enantioselectivities up to 77% were obtained.
Chiral quinolinyl-oxazolines as ligands for copper(I)-catalyzed asymmetric cyclopropanation
Wu, Xin-Yan,Li, Xiang-Hong,Zhou, Qi-Lin
, p. 4143 - 4150 (2007/10/03)
Chiral quinolinyl-oxazoline compounds have been synthesized from enantiomerically pure amino alcohols and 8-quinoline-carboxylic acid using a convenient procedure. Asymmetric cyccopropanation of styrene with diazoacetates in the presence of 1 mol% of CuOTf and quinolinyl-oxazolines gave 2-phenylcyclopropane carboxylates in moderate enantiomeric excesses.
