110548-06-6 Usage
Description
Ethyl (R)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylate is a complex organic ester compound, a member of the quinoline family, characterized by the presence of fluorine atoms at the 9th and 10th positions, a methyl group, and a carboxylate group. ethyl (R)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylate exhibits unique structural features that may confer it with specific pharmacological properties, making it a candidate for medicinal and research applications.
Uses
Used in Pharmaceutical Industry:
Ethyl (R)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylate is used as a potential pharmaceutical agent for [specific medical application, if known] due to its unique chemical structure and pharmacological properties. Its fluorine substitution and quinoline backbone may contribute to its interaction with biological targets, offering therapeutic benefits in treating certain diseases or conditions.
Used in Chemical Research:
In the field of chemical research, ethyl (R)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylate serves as a valuable compound for studying the effects of structural modifications on the properties and activities of organic esters. Its synthesis and modification can provide insights into the development of new drugs and materials with improved efficacy and selectivity.
Check Digit Verification of cas no
The CAS Registry Mumber 110548-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,4 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 110548-06:
(8*1)+(7*1)+(6*0)+(5*5)+(4*4)+(3*8)+(2*0)+(1*6)=86
86 % 10 = 6
So 110548-06-6 is a valid CAS Registry Number.
110548-06-6Relevant articles and documents
Asymmetric metal-free synthesis of fluoroquinolones by organocatalytic hydrogenation
Rueping, Magnus,Stoeckel, Mirjam,Sugiono, Erli,Theissmann, Thomas
experimental part, p. 6565 - 6568 (2010/10/19)
A highly enantioselective organocatalytic transfer hydrogenation enabling the synthesis of both 6-fluoro-2-methyltetrahydroquinoline and 7,8-difluoro-3-methyl-benzoxazine has been developed. These key building blocks can for the first time be synthesized using the same methodology allowing fast and efficient, metal-free access to the antibiotic fluoroquinolones flumequine and levofloxacine.
Synthesis and antibacterial activities of optically active ofloxacin and its fluoromethyl derivative.
Atarashi,Yokohama,Yamazaki,Sakano,Imamura,Hayakawa
, p. 1896 - 1902 (2007/10/02)
-
