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(Z)-3-(3-Bromo-phenyl)-3-morpholin-4-yl-1-phenyl-propenone is a complex organic compound with the molecular formula C20H18BrNO2. It is a derivative of chalcone, featuring a phenyl group, a morpholinyl group, and a bromine atom attached to the phenyl ring. (Z)-3-(3-Bromo-phenyl)-3-morpholin-4-yl-1-phenyl-propenone is characterized by its (Z)-configuration, indicating the geometric arrangement of the double bond, with the phenyl and morpholinyl groups on the same side of the double bond. It is a yellowish solid and is used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. The presence of the bromine atom makes it a valuable building block for further functionalization and modification in organic synthesis.

56300-24-4

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56300-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56300-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,0 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56300-24:
(7*5)+(6*6)+(5*3)+(4*0)+(3*0)+(2*2)+(1*4)=94
94 % 10 = 4
So 56300-24-4 is a valid CAS Registry Number.

56300-24-4Downstream Products

56300-24-4Relevant academic research and scientific papers

KINETIC RELATIONSHIPS OF THE REACTION OF 1,3-DIARYL-1-PROPYN-3-ONES WITH MORPHOLINE AND BUTYLAMINE IN POLAR APROTIC SOLVENTS

Korshunov, S. P.,Slyusareva, O. M.,Korzhova, N. V.,Kazantseva, V. M.

, p. 815 - 819 (2007/10/02)

The kinetics of the reaction of substituted 1,3-diphenyl-1-propyn-3-ones with butylamine and morpholine in acetonitrile and DMFA were studied by a polarographic method in the range of 294-323 deg K with the amines at concentrations (0.05-0.1 mol) securing nondependance of the second-order rate constants on the concentration of the amine.The reactions in acetonitrile and DMFA are characterized by lower ΔH(activ.) values and more negative ΔS(activ.) values than the reactions in alcohol.This is due to the larger degree of separation of the charges and to the solvationstate in the aprotic solvents.It is confirmed by data on the effect of the substituents in the substituted ketones on the rate of their reaction with the amines.

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