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2,4,5-tris(4-chlorophenyl)-1H-imidazole is a complex organic compound with the molecular formula C20H12Cl3N. It is characterized by the presence of three 4-chlorophenyl groups attached to the imidazole ring, which is a heterocyclic aromatic organic compound. 2,4,5-tris(4-chlorophenyl)-1H-imidazole is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique chemical structure and properties. It is important to note that the handling and use of such chemicals should be done with caution, as they may have specific safety and environmental considerations.

1498-38-0

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1498-38-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1498-38-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,9 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1498-38:
(6*1)+(5*4)+(4*9)+(3*8)+(2*3)+(1*8)=100
100 % 10 = 0
So 1498-38-0 is a valid CAS Registry Number.

1498-38-0Downstream Products

1498-38-0Relevant academic research and scientific papers

Preparation method for 2,4,5-trisubstituted imidazole compound

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Paragraph 0021; 0022; 0023; 0024, (2019/03/26)

The invention relates to a preparation method for 2,4,5-trisubstituted imidazole. According to the method, benzylamine is used as a substrate, and ZnIn2S4 is used as a photocatalyst; and under the condition of illumination of visible light, benzylamine un

Efficient synthesis of 2,4,5-triaryl-1H-imidazoles from aromatic aldehydes with HMDS catalyzed by N-bromosaccharin (NBSa)

Sedrpoushan, Alireza,Joshani, Zinab,Fatollahi, Leila

, p. 287 - 292 (2014/05/20)

A one-pot efficient procedure for the synthesis of 2, 4, 5-triaryl-1H-imidazole derivatives by the reactions of hexamethyldisilazane and arylaldehydes in the presence of N-bromosaccharin (NBSa) is studied. This new method offers several advantages, such as excellent yields, easy workup, short reaction times, and simple procedure.

Convenient one-pot synthesis of 2,4,5-triaryl-1H-imidazoles from arylaldehydes, benzyl alcohols, or benzyl halides with HMDS in the presence of molecular iodine

Veisi, Hojat,Khazaei, Ardashir,Heshmati, Leila,Hemmati, Saba

experimental part, p. 1231 - 1234 (2012/07/14)

A one-pot efficient procedure for the synthesis of 2,4,5-triaryl-1 H-imidazole derivatives in good to excellent yields by reaction between hexamethyldisilazane and arylaldehydes, benzyl alcohols, benzyl halides in the presence of molecular iodine has been developed. The remarkable advantages of this method are the simple workup procedure, high yields of products, and the availability of reagents.

One-pot synthesis of 2,4,5-triaryl-1 H -imidazoles from arylaldehydes, benzyl alcohols, or benzyl halides with hexamethyldisilazane in molten tetrabutylammonium bromide

Salehi, Javad,Khodaei, Mohammad M.,Khosropour, Ahmad R.

experimental part, p. 459 - 462 (2011/04/16)

A simple and efficient method for the synthesis of 2,4,5-triaryl-1H- imidazole derivatives in good to excellent yields by reaction between hexamethyldisilazane and arylaldehydes, benzyl alcohols, benzyl halides in molten tetrabutylammonium bromide as an inexpensive and non toxic solvent has been developed. The remarkable advantages of this method are the simple workup procedure, high yields of products, the use of an ionic liquid as a green solvent, and the availability of reagents. Georg Thieme Verlag Stuttgart - New York.

Facile method for one-step synthesis of 2,4,5-triarylimidazoles under catalyst-free, solvent-free, and microwave-irradiation conditions

Zhou, Jian-Feng,Gong, Gui-Xia,Sun, Xiao-Jun,Zhu, Yu-Lan

experimental part, p. 1134 - 1141 (2010/04/29)

A green and efficient method for the synthesis of 2,4,5-triarylimidazoles by one-step condensation reaction of benzil, aromatic aldehyde, and ammonium acetate under catalyst-free, solvent-free, and microwave-irradiation conditions is reported. This method had many dramatic advantages, such as the short reaction time (3-5min), good yields (80-99%), environmental friendliness, and convenient operation.

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