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1,4-Naphthalenedione, 2-chloro-3-[(4-phenyl-2-thiazolyl)amino]- is a complex organic compound with the chemical formula C18H11ClN2OS. It is a derivative of 1,4-naphthoquinone, featuring a 2-chloro-3-amino substitution pattern. The molecule contains a phenyl group attached to a thiazolyl ring, which is further connected to the naphthalene core. 1,4-Naphthalenedione, 2-chloro-3-[(4-phenyl-2-thiazolyl)amino]- is known for its potential applications in the synthesis of dyes and pharmaceuticals, particularly as an intermediate in the production of certain colorants and therapeutic agents. Its chemical structure endows it with unique properties that can be exploited in various chemical reactions and industrial processes.

60463-71-0

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60463-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60463-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60463-71:
(7*6)+(6*0)+(5*4)+(4*6)+(3*3)+(2*7)+(1*1)=110
110 % 10 = 0
So 60463-71-0 is a valid CAS Registry Number.

60463-71-0Downstream Products

60463-71-0Relevant academic research and scientific papers

Synthesis and biological evaluation of 2-chloro-3-[(thiazol-2-yl)amino]-1,4-naphthoquinones

Olawode, Emmanuel O.,Tandlich, Roman,Prinsloo, Earl,Isaacs, Michelle,Hoppe, Heinrich,Seldon, Ronnett,Warner, Digby F.,Steenkamp, Vanessa,Kaye, Perry T.

, p. 1572 - 1575 (2019/05/15)

A series of novel, substituted 2-chloro-3-[(thiazol-2-yl)amino]-1,4-naphthoquinones have been prepared and shown to exhibit promising concentration-dependent activity against human SH-SY5Y cells, Plasmodium falciparum, Mycobacterium tuberculosis and P. aeruginosa. Substituent effects on observed bioactivity have been explored; the para-fluorophenyl derivative 3d exhibited activity across the range of the bioassays employed, indicating the potential of the 2-chloro-3-[(4-arylthiazol-2-yl)amino]-1,4-naphthoquinone scaffold in the development of novel, broad spectrum therapeutics.

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