151213-15-9 Usage
Description
3-Quinolinecarboxylic acid, 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-4-oxo-, (4aS-cis)is a complex organic compound with a unique molecular structure. It belongs to the quinolinecarboxylic acid family and is characterized by its cyclopropyl, difluoro, and octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl moieties. 3-Quinolinecarboxylic acid, 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-4-oxo-, (4aS-cis)exhibits a pale yellow solid appearance and is known for its potential applications in various industries due to its chemical properties.
Uses
Used in Pharmaceutical Industry:
3-Quinolinecarboxylic acid, 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-4-oxo-, (4aS-cis)is used as an active pharmaceutical ingredient (API) for the development of new drugs targeting various diseases. Its unique molecular structure allows it to interact with specific biological targets, making it a promising candidate for drug discovery and development.
Used in Chemical Research:
In the field of chemical research, this compound serves as a valuable research tool for understanding the structure-activity relationships of quinolinecarboxylic acid derivatives. It can be used to study the effects of different functional groups on the biological activity and pharmacokinetic properties of the molecule, contributing to the advancement of scientific knowledge in medicinal chemistry.
Used in Material Science:
The unique chemical properties of 3-Quinolinecarboxylic acid, 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-4-oxo-, (4aS-cis)make it a potential candidate for the development of new materials with specific properties. It can be explored for its potential applications in areas such as optoelectronics, sensors, and advanced materials.
Used in Agricultural Industry:
3-Quinolinecarboxylic acid, 1-cyclopropyl-6,8-difluoro-1,4-dihydro-7-(octahydro-6H-pyrrolo[3,4-b]pyridin-6-yl)-4-oxo-, (4aS-cis)may also find applications in the agricultural industry, where it can be used as a starting material for the synthesis of new pesticides or herbicides. Its unique chemical structure could potentially provide novel modes of action against pests and weeds, contributing to more effective and sustainable agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 151213-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,2,1 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 151213-15:
(8*1)+(7*5)+(6*1)+(5*2)+(4*1)+(3*3)+(2*1)+(1*5)=79
79 % 10 = 9
So 151213-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H21F2N3O3/c21-14-6-12-17(25(11-3-4-11)8-13(19(12)26)20(27)28)16(22)18(14)24-7-10-2-1-5-23-15(10)9-24/h6,8,10-11,15,23H,1-5,7,9H2,(H,27,28)/t10-,15+/m0/s1
151213-15-9Relevant articles and documents
Method for synthesizing moxifloxacin and derivatives thereof
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Paragraph 0046-0050, (2019/10/01)
The invention provides a method for synthesizing moxifloxacin and derivatives thereof. Aminopyrrolidone derivatives are constructed to further obtain (S,S)-2,8-diazo-bicyclo[4.3.0]nonane so as to synthesize the moxifloxacin and the derivatives thereof. The method has the beneficial effects that raw materials are wide in source and low in price; chiral resolution is not needed in a preparation process; the yield and purity are relatively high; the process cost is further reduced; obvious economic value is achieved.
7-(1-PYRROLIDINYL)-3-QUINOLONE-AND-NAPHTHYRIDONECARBOXYLIC ACID DERIVATIVES AS ANTIBACTERIAL AGENTS AND FEED ADDITIVES
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, (2008/06/13)
7-(1-Pyrrolidinyl)-3-quinolone- and -naphthyridonecarboxylic acid derivatives as antibacterial agents and feed additives, of the formula in which X1 is halogen, X2 is hydrogen, halogen, amino or other radical, R1 is alkyl, cycloalkyl, optionally substituted phenyl or other radical, R2 is hydrogen, alkyl or a dioxolylmethyl radical, R 3 i s A is N, CH, C-halogen, or the like, or forms a bridge with R1, and addition products thereof
