623144-25-2 Usage
Type of compound
Trifluoromethanesulfonate salt
A salt derived from trifluoromethanesulfonic acid, which is a strong acid and a useful reagent in organic synthesis.
Derivative
Quinoline
A heterocyclic aromatic compound with a nitrogen atom in the ring structure, which is the basis for the structure of the 2-(2,6-dichlorophenyl)-6-quinolinyl trifluoromethanesulfonate.
Application
Reagent in organic synthesis
Commonly used in chemical reactions to facilitate or promote the formation of desired products.
Complex formation
Stable complexes with various metal ions
The compound is known for its ability to form stable complexes with different metal ions, which can be beneficial in catalytic processes and metal-mediated reactions.
Potential use
Development of new pharmaceuticals and agrochemicals
The compound has been studied for its possible applications in creating new drugs and agricultural chemicals due to its unique properties and reactivity.
Safety concerns
Health and environmental hazards
It is important to handle 2-(2,6-dichlorophenyl)-6-quinolinyl trifluoromethanesulfonate with caution, as it may pose risks to human health and the environment if not properly managed or disposed of.
Check Digit Verification of cas no
The CAS Registry Mumber 623144-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,3,1,4 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 623144-25:
(8*6)+(7*2)+(6*3)+(5*1)+(4*4)+(3*4)+(2*2)+(1*5)=122
122 % 10 = 2
So 623144-25-2 is a valid CAS Registry Number.
623144-25-2Relevant academic research and scientific papers
2,6-Quinolinyl derivatives as potent VLA-4 antagonists
Lassoie, Marie-Agnes,Broeders, Fabienne,Collart, Philippe,Defrere, Laurent,de Laveleye-Defais, Francoise,Demaude, Thierry,Gassama, Abdoulaye,Guillaumet, Gerald,Hayez, Jean-Claude,Kiss, Laszlo,Knerr, Laurent,Nicolas, Jean-Marie,Norsikian, Stephanie,Quere, Luc,Routier, Sylvain,Verbois, Valerie,Provins, Laurent
, p. 142 - 146 (2007/10/03)
A new series of 2,6-quinolinyl derivatives was prepared leading to potent low nanomolar VLA-4/VCAM-1 antagonists.
2,6-QUINOLINYL AND 2,6-NAPHTHYL DERIVATIVES, PROCESSES FOR PREPARING THEM AND THEIR USES AS VLA-4 INHIBITORS
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Page/Page column 58, (2010/02/07)
The present invention concerns 2,6-quinolinyl and 2,6-naphthyl derivatives of formula (I), processes for preparing them, pharmaceutical compositions containing them and their use as pharmaceuticals for the treatment of VLA-4 dependent inflammatory diseases such as for example asthma, allergic rhinitis, sinusitis, conjunctivitis, food allergy, psoriasis, urticaria, pruritus, eczema, rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis and atherosclerosis. Formula (I): wherein X is N or CH.
