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2-(2-piperidinylethyl)-1H-isoindole-1,3(2H)-dione is a complex organic compound with the molecular formula C16H20N2O2. It is a derivative of the isoindole-1,3-dione structure, which is characterized by a fused six-membered ring system containing two carbonyl groups. The compound features a piperidinylethyl side chain attached to the 2-position of the isoindole core, providing additional nitrogen atoms and contributing to its overall structure. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly those with biological activity. Its specific properties, such as solubility, stability, and reactivity, can be influenced by the presence of the piperidinyl group, making it a versatile building block in organic synthesis.

4667-75-8

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4667-75-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4667-75-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4667-75:
(6*4)+(5*6)+(4*6)+(3*7)+(2*7)+(1*5)=118
118 % 10 = 8
So 4667-75-8 is a valid CAS Registry Number.

4667-75-8Relevant academic research and scientific papers

REACTION OF N-SUBSTITUTED PHTHALIMIDES AND ISOPHTHALIMIDES WITH SECONDARY AMINES

Ganin, E. V.,Makarov, V. F.,Rozynov, B. V.

, p. 2205 - 2208 (2007/10/02)

The N,N'-substituted diamides of phthalic acid are formed in the reaction of N-substituted phthalimides and isophthalimides with secondary amines.The isophthalimides are stronger agents.Cyclic amines with a medium ring size are acylated so readily that the reaction of 2-bromoethylphthalimide with piperidine leads primarily to the acylation product.

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