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8-Cinnamoyloxyquinoline is a chemical compound with the molecular formula C18H13NO2. It is a derivative of quinoline, a heterocyclic aromatic compound, and features a cinnamoyl group (a type of ester derived from cinnamic acid) attached to the 8-position of the quinoline ring. 8-cinnamoyloxyquinoline is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique chemical structure and properties. It can be synthesized through various chemical reactions and is often used as an intermediate in the preparation of more complex molecules. The compound's specific applications and properties can vary depending on the context in which it is used, highlighting its versatility in chemical research and development.

5296-42-4

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5296-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5296-42-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5296-42:
(6*5)+(5*2)+(4*9)+(3*6)+(2*4)+(1*2)=104
104 % 10 = 4
So 5296-42-4 is a valid CAS Registry Number.

5296-42-4Relevant academic research and scientific papers

CHIMIE DES SUCRES SANS GROUPEMENTS PROTECTEURS-I-ESTERIFICATION REGIOSELECTIVE DE L'HYDROXYLE ANOMERE DU LACTOSE, DU MALTOSE ET DU GLUCOSE

Plusquellec, Daniel,Roulleau, Fabienne,Bertho, Francoise,Lefeuvre, Martine,Brown, Eric

, p. 2457 - 2468 (1986)

Treatment of acyl chlorides 4 with mercaptothiazoline, mercaptobenzothiazole, p-nitrophenol and 8-hydroxyquinoline in the presence of Et3N, afforded high yields of the corresponding reactive amides 5a-h,S-thioesters 6e-h and aryl esters 7e-h and 8a-h, respectively.The esters 6e-h, 7e-h and 8e-h reacted with excess β-lactose in pyridine, to give the corresponding β-esters 9e-h resulting from esterification of the anomeric hydroxyl of the sugar.The amides 5c, f-h gave the α-lactosyl esters 9c, f-h.The amide 5e and the esters 8b, c, e reacted with β-maltose, thus affording the corresponding β-maltosyl esters 10b, c, e, whereas the compounds 8a-e reacted with β-glucose, yielding the corresponding β-glucosyl esters 11a-e.This appears to be one of the very few selective chemical modifications of sugars known, which do not involve the toilsome protection-deprotection methology.The now commercially available maltosyl and glucosyl esters 10e and 11d-e are new non-ionic, and water soluble detergents which could be used for studies of cell membrane proteins.

NMR study of O and N, O-substituted 8-quinolinol derivatives

Mastoor, Sobia,Faizi, Shaheen,Saleem, Rubeena,Siddiqui, Bina Shaheen

, p. 115 - 121 (2014/03/21)

The 1H and 13C NMR spectral study of several biologically active derivatives of 8-quinolinol have been made through extensive NMR studies including homodecoupling and 2D-NMR experiments such as COSY-45°, NOESY, and HeteroCOSY. Electron donating resonance and electron withdrawing inductive effect of several groups showed marked changes in chemical shifts of nuclei at the seventh positions of O-substituted quinolinols (2-15). Although in N-alkyl, 8-alkoxyquinolinium halides (16-21), ring A rightly showed low frequency chemical shift values. Copyright

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