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N-hydroxy-2,4,6-trimethyl-N'-phenyl-benzamidine is an organic compound with the molecular formula C15H16N2O. It is a derivative of benzamidine, featuring a hydroxyl group (-OH) attached to the nitrogen atom, and three methyl groups (-CH3) at the 2, 4, and 6 positions of the benzene ring. The molecule also contains a phenyl group (C6H5) attached to the other nitrogen atom. N-hydroxy-2,4,6-trimethyl-N'-phenyl-benzamidine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as a reagent in chemical reactions. Due to its reactivity and the presence of functional groups, it is often used in the preparation of complex organic molecules and as an intermediate in the production of certain dyes and pigments.

3023-19-6

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3023-19-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3023-19-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3023-19:
(6*3)+(5*0)+(4*2)+(3*3)+(2*1)+(1*9)=46
46 % 10 = 6
So 3023-19-6 is a valid CAS Registry Number.

3023-19-6Relevant academic research and scientific papers

KINETICS OF THE ACID-CATALYSED ADDITION OF ARYLAMINES TO AROMATIC NITRILE OXIDES

Beltrame, Paolo,Daga, Caterina,Gelli, Gioanna

, p. 15 - 20 (2007/10/02)

The addition of arylamines to stable aromatic nitrile oxides, giving rise to substituted N-arylbenzamidoximes, was carried out in carbon tetrachloride, in the presence of acetic acid as catalyst.Kinetic measurements were done at 30.3 deg C.Attention was paid to the term in the rate equation which corresponds to the catalysed reaction: the observed kinetic effect of substituents on the nitrile oxide and on the aniline benzene rings suggests a concerted attack of arylamine and acetic acid on to ArCNO as the most probable reaction mechanism.

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