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4,4-Dimethyl-1-phenylpyrrolidin-2-one is a chemical compound with the molecular formula C12H15NO. It is a white crystalline solid that belongs to the class of pyrrolidinone derivatives. 4,4-dimethyl-1-phenylpyrrolidin-2-one is characterized by the presence of a pyrrolidinone ring, which is a five-membered heterocyclic ring containing one nitrogen atom, and a phenyl group attached to the nitrogen. The two methyl groups at the 4-position of the pyrrolidinone ring contribute to its stability and lipophilicity. 4,4-Dimethyl-1-phenylpyrrolidin-2-one is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of sedatives, hypnotics, and muscle relaxants. Its chemical properties and reactivity make it a valuable building block in organic synthesis, allowing for the creation of a wide range of complex molecules with potential therapeutic applications.

2996-60-3

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2996-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2996-60-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2996-60:
(6*2)+(5*9)+(4*9)+(3*6)+(2*6)+(1*0)=123
123 % 10 = 3
So 2996-60-3 is a valid CAS Registry Number.

2996-60-3Downstream Products

2996-60-3Relevant academic research and scientific papers

Minimization of Back-Electron Transfer Enables the Elusive sp3 C?H Functionalization of Secondary Anilines

Zhao, Huaibo,Leonori, Daniele

, p. 7669 - 7674 (2021)

Anilines are some of the most used class of substrates for application in photoinduced electron transfer. N,N-Dialkyl-derivatives enable radical generation α to the N-atom by oxidation followed by deprotonation. This approach is however elusive to monosubstituted anilines owing to fast back-electron transfer (BET). Here we demonstrate that BET can be minimised by using photoredox catalysis in the presence of an exogenous alkylamine. This approach synergistically aids aniline SET oxidation and then accelerates the following deprotonation. In this way, the generation of α-anilinoalkyl radicals is now possible and these species can be used in a general sense to achieve divergent sp3 C?H functionalization.

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