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(4-Nitro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetic acid N'-phenyl-hydrazide is a complex organic compound with the molecular formula C16H12N4O5. It is characterized by a 4-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-yl group attached to an acetic acid moiety, which is further connected to a phenyl-hydrazide group. (4-Nitro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-acetic acid N'-phenyl-hydrazide is known for its potential applications in pharmaceutical research, particularly as a building block for the synthesis of various biologically active molecules. Its structure features a nitro group, which can be reduced to an amine group under certain conditions, making it a versatile intermediate in the synthesis of drugs and other chemical entities. The compound's properties, such as solubility and reactivity, can be influenced by the presence of the nitro group and the phenyl-hydrazide moiety, which can participate in various chemical reactions, including reduction, substitution, and condensation reactions.

91626-80-1

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91626-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91626-80-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,2 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91626-80:
(7*9)+(6*1)+(5*6)+(4*2)+(3*6)+(2*8)+(1*0)=141
141 % 10 = 1
So 91626-80-1 is a valid CAS Registry Number.

91626-80-1Downstream Products

91626-80-1Relevant academic research and scientific papers

Acid Acides: Part IX - Synthesis and Reactions of Phthalimidoacetic Acid Azide and Its Derivatives

Aly, N. F.,Fahmy, A. F. M.,Mahmoud, M.,Arief, M. H.,Elkoumy, M. A.

, p. 121 - 124 (2007/10/02)

Azides (IIa-c), prepared from the corresponding acid chlorides (Ia-c), on base-catalyzed decomposition with aromatic amines and aminobezoic acids give the corresponding N-aryl-N'-(phthalimidomethyl)ureas (IVa-u) via Curtius rearrangement.However, the base-catalyzed decomposition of II with hydrazines takes place via azido-group displacement to give the corresponding hydrazides (VIa-f).Lewis acid (AlCl3)-catalyzed decomposition of IIa-c in aromatic substrates gives N-aroylphthalimidomethyl amines (IXa-g).

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