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4,5,6-trifluoro-2-nitro-1,3-phenylenediamine is an organic compound with the molecular formula C6H3F3N4O2. It is a derivative of phenylenediamine, featuring three fluorine atoms at the 4, 5, and 6 positions, and a nitro group at the 2 position. 4,5,6-trifluoro-2-nitro-1,3-phenylenediamine is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its unique structure and reactivity. The presence of fluorine atoms can significantly influence the compound's properties, such as its lipophilicity and metabolic stability, which are important factors in drug design. The nitro group provides additional functional groups for further chemical reactions, making 4,5,6-trifluoro-2-nitro-1,3-phenylenediamine a versatile building block in organic synthesis.

2106-01-6

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2106-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2106-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2106-01:
(6*2)+(5*1)+(4*0)+(3*6)+(2*0)+(1*1)=36
36 % 10 = 6
So 2106-01-6 is a valid CAS Registry Number.

2106-01-6Relevant academic research and scientific papers

Polyhalogenonitrobenzenes and derived compounds: Part 5. Improved preparations of 1,2,3,4-tetrafluoro-5,6-dinitrobenzene and 3,4,5,6-tetrafluoro-1,2-phenylenediamine, and the use of the latter for the synthesis of tetrafluorobenzheterocycles

Heaton, Alan,Hill, Mark,Drakesmith, Frederick

, p. 133 - 138 (1997)

The preparation of 2,3,4,5-tetrafluoro-6-nitroaniline (3) by amination of pentafluoronitrobenzene has been speeded up, scaled up and the yield increased by controlling the reaction by TLC monitoring and using 'dry column' chromatography. Compound (3) was readily converted to 1,2,3,4-tetrafluoro-5,6-dinitrobenzene (2) by peroxytrifluoroacetic acid and to 3,4,5,6-tetrafluoro-1,2-phenylenediamine (1) by SnCl2/HCl, Compound (1) was shown to be a versatile intermediate for the synthesis of tetrafluoro-benzimidazoles, -triazoles and -quinoxalines. The fungicidal activity of the latter are reported here.

REACTION OF AROMATIC COMPOUNDS WITH NUCLEOPHILIC REAGENTS IN LIQUID AMMONIA. X. AMINATION OF POLYFLUORINATED AROMATIC COMPOUNDS CONTAINING ELECTRON-WITHDRAWING SUBSTITUENTS

Selivanova, G. A.,Chuikova, T. V.,Shtark, A. A.,Shteingarts, V. D.

, p. 2267 - 2272 (2007/10/02)

It was shown for the case of 2,4-difluoro-, 2,4,6-trifluoro-, and pentafluoronitrobenzenes that both liquid ammonia and sodium amide in liquid ammonia are effective reagents for aminodefluorination with respect to the fluorine derivatives of nitrobenzene.The observed tendency for the ortho-orientation with respect to the nitro group to change to para-orientation with increase in the number of fluorine atoms is more clearly defined for sodium amide than for liquid ammonia as nucleophile on account, clearly, of the stabilization of the transition state of ortho-substitution in the latter case by an intramolcular hydrogen bond.

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