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(E)-2-(2-phenylethenyl)-1,3-dinitrobenzene is an organic compound characterized by a benzene ring with two nitro groups at the 1 and 3 positions and a 2-phenylethenyl group attached at the 2 position. This molecule features a double bond between the phenyl group and the benzene ring, which gives it the "E" configuration, indicating the trans arrangement of the substituents around the double bond. The compound is known for its potential applications in the synthesis of various organic compounds and as a chemical intermediate. It is important to note that due to the presence of nitro groups, (E)-2-(2-phenylethenyl)-1,3-dinitrobenzene may exhibit explosive properties and should be handled with caution.

98751-32-7

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98751-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98751-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,5 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 98751-32:
(7*9)+(6*8)+(5*7)+(4*5)+(3*1)+(2*3)+(1*2)=177
177 % 10 = 7
So 98751-32-7 is a valid CAS Registry Number.

98751-32-7Downstream Products

98751-32-7Relevant academic research and scientific papers

Mild Synthesis of Polyfunctional Benzimidazoles and Indoles by the Reduction of Functionalized Nitroarenes with Phenylmagnesium Chloride

Dohle, Wolfgang,Staubitz, Anne,Knochel, Paul

, p. 5323 - 5331 (2007/10/03)

Phenylmagnesium chloride has been used for the conversion of selected nitroarenes into nitrenes. Their insertion into a neighboring sp2 C-H bond yielded functionalized heterocycles. A novel and mild synthesis of polyfunctional benzimidazoles and indoles is described.

Arylation with 1,3-Dinitroarenes and Copper(I) t-Butoxide. Scope and Limitations

Carter, Stephen D.,Wallace, Timothy W.

, p. 1601 - 1633 (2007/10/02)

The reaction of 1,3-dinitrobenzene with copper(I) t-butoxide and an iodoarene, which produces a 2,6-dinitrobiphenyl, has been stidied in detail with a variety of substrates.Iodoarenes containing ester, aldehyde, or other halogen functions were effective, but replacement of the iodoarene with a bromoarene, iodoalkyne, or iodoalkene resulted in less efficient coupling, promoting side-reactions.On replacing the second nitro group on the dinitrobenezene with nitrile, ester, amide, or trifluoromethyl groups, little or no coupling was observed.Limiting side-reactions usually involved the decomposition of substrates by t-butoxide via nucleophilic substitution, elimination, or deprotonation.A mechanism based on reversible cupration of the dinitroarene is proposed.

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