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2-Nitro-6-nitroso-4-trifluoromethylaniline is a complex organic chemical compound characterized by its molecular formula C7H4F3N4O4. 2-nitro-6-nitroso-4-trifluoromethylaniline features a trifluoromethyl group (-CF3) attached to the aniline (C6H5NH2) structure, with nitro groups (-NO2) at the 2nd and 6th positions, and a nitroso group (-NO) at the 4th position. The presence of these functional groups endows the molecule with unique chemical properties, such as high reactivity and potential applications in the synthesis of pharmaceuticals, dyes, and other specialty chemicals. Due to its complex structure and the presence of multiple nitro and nitroso groups, 2-nitro-6-nitroso-4-trifluoromethylaniline may exhibit hazardous properties, necessitating careful handling and storage in accordance with safety regulations.

6574-18-1

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6574-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6574-18-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6574-18:
(6*6)+(5*5)+(4*7)+(3*4)+(2*1)+(1*8)=111
111 % 10 = 1
So 6574-18-1 is a valid CAS Registry Number.

6574-18-1Downstream Products

6574-18-1Relevant academic research and scientific papers

O-Nitroaniline derivatives. Part 14. Cyclisations leading to benzimidazole N-oxides, N-hydroxybenzimidazolones and N-hydroxyquinoxaline-2,3-diones: A mechanistic borderline

Collins Cafiero, Pamela A.,French, Colin S.,McFarlane, Michael D.,Mackie, Raymond K.,Smith, David M.

, p. 1375 - 1384 (2007/10/03)

The base-induced cyclisations of N-(o-nitrophenyl)glycine derivatives (nitriles 9 or esters 13) bearing additional substituents at the other ortho-position are anomalous, resembling those involving N-(o-nitrophenyl)sarcosine analogues. The nitriles are co

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