56595-09-6 Usage
Uses
Used in Pharmaceutical Industry:
Quinazoline, 4-fluoro(9CI) is utilized as a key intermediate in the synthesis of new medicines and pharmaceutical compounds. Its presence of the fluorine atom endows it with distinctive properties and reactivity, making it a valuable component in the development of innovative drug formulations.
Used in Organic Synthesis:
In the realm of organic synthesis, Quinazoline, 4-fluoro(9CI) is employed as an important intermediate. Its unique structure and reactivity contribute to the creation of a variety of complex organic molecules, further expanding its applications in research and development.
Used in Research and Development:
Quinazoline, 4-fluoro(9CI) holds potential in various research areas, particularly in the exploration of new chemical entities and the advancement of pharmaceutical sciences. Its unique characteristics make it a promising candidate for the discovery of novel therapeutic agents and the enhancement of existing drug compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 56595-09-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,9 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56595-09:
(7*5)+(6*6)+(5*5)+(4*9)+(3*5)+(2*0)+(1*9)=156
156 % 10 = 6
So 56595-09-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5FN2/c9-8-6-3-1-2-4-7(6)10-5-11-8/h1-5H
56595-09-6Relevant articles and documents
Rhodium-catalyzed transformation of heteroaryl aryl ethers into heteroaryl fluorides
Arisawa, Mieko,Tanii, Saori,Tazawa, Takeru,Yamaguchi, Masahiko
supporting information, p. 11390 - 11393 (2016/09/23)
A rhodium complex catalyzed the conversion of the C-O bond of heteroaryl aryl ethers to the C-F bond. The reaction of (4-chlorophenylthio)pentafluorobenzene with heteroaryl aryl ethers provided heteroaryl fluorides and heteroaryl (4-chlorophenylthio)tetrafluorophenyl ethers; this involved the cleavage of a single heteroaryl C-O bond under equilibrium conditions. The reaction of heteroaryl aryl ethers with 2-fluorobenzothiazole in which two heteroaryl and aryl C-O bonds were cleaved provided heteroaryl fluorides and aryl fluorides. The reactions were applicable to five-membered and six-membered heteroaryl aryl ethers and also to diaryl ethers possessing one or two electron-withdrawing groups.
