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N,N'-(5-(trifluoromethyl)-1,3-phenyl)bisacetamide is a complex organic compound with the molecular formula C12H10F3N2O2. It is characterized by a central 1,3-phenyl backbone, which is a benzene ring with two carbon atoms at positions 1 and 3. Attached to the 5-position of this phenyl ring is a trifluoromethyl group (-CF3), which introduces three fluorine atoms. The compound is further defined by two acetamide groups (-CONH2), each connected to the nitrogen atoms of the phenyl ring. These acetamide groups contribute to the compound's amide character, which can influence its reactivity and properties. The presence of fluorine atoms in the trifluoromethyl group can significantly affect the compound's lipophilicity, electronic properties, and potential applications in various chemical and pharmaceutical contexts.

349-61-1

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349-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 349-61-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,4 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 349-61:
(5*3)+(4*4)+(3*9)+(2*6)+(1*1)=71
71 % 10 = 1
So 349-61-1 is a valid CAS Registry Number.

349-61-1Downstream Products

349-61-1Relevant academic research and scientific papers

Photochemical reactivity of trifluoromethyl aromatic amines: The example of 3,5-diamino-trifluoromethyl-benzene (3,5-DABTF)

Chaignon, Philippe,Cortial, Sylvie,Guerineau, Vincent,Adeline, Marie-Therese,Giannotti, Charles,Fan, Gerard,Ouazzani, Jamal

, p. 1539 - 1543 (2005)

This work presents the application of an on-line photoreactor to the detection of 3,5-diamino-trifluoromethyl-benzene (3,5-DABTF) in aqueous solutions. When irradiated at 310 nm, this compound is defluorinated to 3,5-diaminobenzoic acid by a nucleophilic substitution of the fluoride by water. Concomitantly, defluorination intermediates polymerize through amide bonds to give dark-colored compounds. We take advantage of the photocatalyzed defluorination and the subsequent decrease in pH to develop an original and specific photoreactor. Continuous recording of pH and temperature in the outlet of the reactor by a dual electrode gives us an opportunity to optimize the system. In the photoreactor, 3,5-DABTF is immediately and totally transformed as attested by the rapid drop of the flowing solution pH from 6.2 to 3.2 and the chromatographic analysis of the outgoing solutions. The detection remains effective from 1 to 1000 parts per million.

Method for synthesizing 3-(4-methyl-1H-imidazole-1-yl)-5-(trifluoromethyl) aniline

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Paragraph 0029-0031, (2020/10/14)

The invention relates to a method for synthesizing 3-(4-methyl-1H-imidazole-1-yl)-5-(trifluoromethyl) aniline, which comprises the following steps: 1, by using 3,5-diaminobenzotrifluoride as a raw material, carrying out protection to obtain a mono-substituted product and an intermediate byproduct; and 2, carrying out a cyclization reaction on the mono-substituted product, and carrying out deprotection to obtain the 3-(4-methyl-1H-imidazole-1-yl)-5-(trifluoromethyl) aniline. The synthesis process is safe and reliable, and has the advantages of low cost, easy control of reaction, simple post-treatment, economy, environmental protection and the like.

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