20409-63-6 Usage
Description
(2-nitrophenyl)(thiophen-2-yl)methanone is a chemical compound with the molecular formula C12H8N2O3S. It is composed of a nitrophenyl group, a thiophen-2-yl group, and a methanone group. (2-nitrophenyl)(thiophen-2-yl)methanone possesses a unique structure and properties that make it valuable in various applications.
Uses
Used in Organic Synthesis:
(2-nitrophenyl)(thiophen-2-yl)methanone is used as a building block in the synthesis of more complex organic compounds. Its unique structure allows it to be a versatile component in creating a wide range of organic molecules.
Used in Pharmaceutical Applications:
(2-nitrophenyl)(thiophen-2-yl)methanone is used as a reagent in chemical reactions for the development of new materials and drugs in the field of organic chemistry. Its potential use in pharmaceuticals stems from its ability to contribute to the creation of novel therapeutic agents.
Used in Chemical Reactions:
(2-nitrophenyl)(thiophen-2-yl)methanone is used as a reagent in various chemical reactions, facilitating the synthesis of new compounds and aiding in the advancement of organic chemistry research.
Check Digit Verification of cas no
The CAS Registry Mumber 20409-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,0 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20409-63:
(7*2)+(6*0)+(5*4)+(4*0)+(3*9)+(2*6)+(1*3)=76
76 % 10 = 6
So 20409-63-6 is a valid CAS Registry Number.
20409-63-6Relevant articles and documents
Cascade synthesis of 3-quinolinecarboxylic ester via benzylation/ propargylation-cyclization
Fan, Jinmin,Wan, Changfeng,Sun, Gaojun,Wang, Zhiyong
supporting information; scheme or table, p. 8608 - 8611 (2009/04/04)
(Chemical Equation Presented) Reactions of 2-amino-aryl alcohols with β-ketoesters catalyzed by a catalytic amout of FeCl3 via tandem benzylation-cyclization produce the corresponding 3-quinolinecarboxylic esters in good to high yields. Extending this methodology to propargylation- cyclization, 2-nitrophenyl propargyl alcohols with β-ketoesters catalyzed by FeCl3 and SnCl2 also produce the 4-alkyne-3- quinolinecarboxylic esters. The mechanistic details of this benzylation/ propargylation and cyclization cascade process are also discussed.
