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4-pentyloxybenzylidene-4'-chloroaniline is a complex organic chemical compound with the molecular formula C18H20ClNO. It is characterized by a benzylidene group (a carbon-carbon double bond between a benzene ring and a carbonyl group) connected to a 4-pentyloxybenzene moiety, which in turn is linked to a 4'-chloroaniline group. 4-pentyloxybenzylidene-4'-chloroaniline is known for its potential applications in the synthesis of dyes and pigments, particularly those with specific color properties. The presence of the chlorine atom and the alkoxy group contributes to its reactivity and solubility, making it a valuable intermediate in the chemical industry.

5219-47-6

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5219-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5219-47-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5219-47:
(6*5)+(5*2)+(4*1)+(3*9)+(2*4)+(1*7)=86
86 % 10 = 6
So 5219-47-6 is a valid CAS Registry Number.

5219-47-6Downstream Products

5219-47-6Relevant academic research and scientific papers

Synthesis and antimicrobial activity of 1-(p-substituted)phenyl-3-(p-alkoxy)phenyl-4-phenyl-azetidin-2-ones

Vittoria Diurno,Cristinziano,Mazzoni,Piscopo,Bolognese

, p. 143 - 148 (2007/10/02)

A series of 1-(p-substituted)phenyl)-3-(p-alkoxy)phenyl-4-phenyl-azetidin-2-ones 1a-20a, was synthesized and characterized. Their antimicrobial activity, against Gram+ and Gram - bacteria and Fungi, was tested. The compounds 8a, 13a, 14a, 18a and 6a, 9a,

Liquid Crystalline Properties of N-(4-Alkoxybenzylidene)-4-halogenoanilines

Sakagami, Sakumitsu,Nakamizo, Minoru

, p. 265 - 266 (2007/10/02)

N-(4-alkoxybenzylidene)-4-halogenoanilines have been synthesized, and phase transitions determined using a differential scanning calorimeter and a polarizing microscope.Smectic and nematic phases have been observed for fluoro and chloro derivatives whereas bromo and iodo derivatives exhibit only a smectic phase.

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