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2-(2',4'-dinitroanilino)benzaldehyde is an organic compound with the chemical formula C13H9N3O5. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. 2-(2',4'-dinitroanilino)benzaldehyde is primarily used as a reagent in chemical analysis, particularly for the detection and determination of primary amines. It functions as a chromogenic reagent, undergoing a color change upon reaction with amines, which can be used to identify their presence or quantify their concentration. The compound is also known for its potential applications in the synthesis of dyes and pharmaceuticals, although its use in these areas is less common. It is important to handle 2-(2',4'-dinitroanilino)benzaldehyde with care due to its potential toxicity and the need for proper safety precautions in a laboratory setting.

79110-07-9

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79110-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79110-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,1 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79110-07:
(7*7)+(6*9)+(5*1)+(4*1)+(3*0)+(2*0)+(1*7)=119
119 % 10 = 9
So 79110-07-9 is a valid CAS Registry Number.

79110-07-9Downstream Products

79110-07-9Relevant academic research and scientific papers

The Preparation of Some 2-Nitroacridines and Related Compounds

Rosevear, Judi,Wilshire, John F. K.

, p. 839 - 853 (2007/10/02)

The reaction of 2-fluoro-5-nitrobenzaldehyde with a wide variety of arylamines gives, in general, mixtures of the corresponding 2-arylamino-5-nitrobenzaldehydes and their related anils.Both aldehydes and anils readily underwent acid-catalysed cyclization to give the corresponding 2-nitroacridines.The effect of substituent on the rate of cyclization of these aldehydes and of some related anilino-benzaldehydes and -acetophenones has been studied in trifluoroacetic acid solution by means of 1H n.m.r. spectroscopy.A solution of 2-(N-methylanilino)-5-nitrobenzaldehydein trifluoroacetic acid appears to contain a substituted acridinium ion; treatment of this solution with alkali gave 10-methyl-2-nitroacridone. 1H n.m.r. data for a wide variety of substituted 2-nitroacridines are discussed.

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