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1,4-Naphtoquinon-mono(4-ethyl-2-(methylsulfonylamino)ethyl)amino-2-methylphenylimin is a complex organic compound with the chemical formula C21H24N2O3S. It is a derivative of 1,4-naphthoquinone, which is a type of quinone with a naphthalene ring structure. The compound features a naphthalene core with a quinone group at positions 1 and 4, and a mono-imine functional group attached to the 4-position. The imine group is formed by the condensation of 4-ethyl-2-(methylsulfonylamino)ethylamine with 2-methylphenyl. 1,4-Naphtochinon-mono(4-amino>-2-methylphenylimin) is known for its potential applications in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of certain antitumor agents. Its chemical structure and properties make it a subject of interest in organic chemistry and medicinal chemistry research.

4704-41-0

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4704-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4704-41-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4704-41:
(6*4)+(5*7)+(4*0)+(3*4)+(2*4)+(1*1)=80
80 % 10 = 0
So 4704-41-0 is a valid CAS Registry Number.

4704-41-0Downstream Products

4704-41-0Relevant academic research and scientific papers

TLC analysis of plant peroxides with modifications of the Huber and Frohlke reagent

Rucker,Neugebauer,Kiefer

, p. 601 - 603 (2007/10/02)

With ascaridole (1) as reference compound the reaction mechanism of the peroxide reagent by Huber and Frohlke was investigated. A blue dye formed was isolated and its structure elucidated. By modification of the reagent, the application for the densitometric assay of 1 in chenopodium oil and of the allergen α-peroxyachifolid in yarrow (Achillea millefolium L.) is reported.

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