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2-(2,5-dimethoxyphenyl)-2-methylpropanenitrile is a chemical compound with the molecular formula C12H15NO2. It is an aromatic nitrile derivative, characterized by the presence of a nitrile group (-CN) and a 2,5-dimethoxyphenyl group. 2-(2,5-dimethoxyphenyl)-2-methylpropanenitrile is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and other specialty chemicals. Its structure features a methyl group attached to a propene chain, which is further connected to a phenyl ring substituted with two methoxy groups at the 2nd and 5th positions. The compound's properties, such as its reactivity and solubility, are influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

23023-26-9

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23023-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23023-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,2 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23023-26:
(7*2)+(6*3)+(5*0)+(4*2)+(3*3)+(2*2)+(1*6)=59
59 % 10 = 9
So 23023-26-9 is a valid CAS Registry Number.

23023-26-9Relevant academic research and scientific papers

Preparation of Indolenines via Nucleophilic Aromatic Substitution

Huber, Florian,Roesslein, Joel,Gademann, Karl

supporting information, p. 2560 - 2564 (2019/03/19)

An unusual aromatic substitution to access indolenines is described. 2-(2-Methoxyphenyl)acetonitrile derivatives are reacted with various alkyl and aryl Li reagents to furnish the corresponding indolenine products, constituents of natural products, and cyanine dyes such as indocyanine green. This new method was used to synthesize 41 indolenines with large functional group tolerance, and selected examples were further converted to the corresponding indolenine dyes. Key experiments provide insight into the mechanism of this nucleophilic aromatic substitution.

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