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2,2,4,4-Tetramethyl-1-phenylcarbamoyl-pyrrolidin, also known as 2,2,4,4-tetramethyl-1-phenylcarbamoylpyrrolidine, is an organic compound with the chemical formula C16H24N2O. It is a derivative of pyrrolidine, featuring a phenylcarbamoyl group attached to the nitrogen atom and two methyl groups on each of the two remaining carbons. 2,2,4,4-Tetramethyl-1-phenylcarbamoyl-pyrrolidin is characterized by its molecular structure, which includes a five-membered pyrrolidine ring with two methyl groups on adjacent carbons and a phenyl group attached to the nitrogen atom through a carbamoyl linkage. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and chemical compounds due to its unique structure and reactivity.

76613-38-2

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76613-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76613-38-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,6,1 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76613-38:
(7*7)+(6*6)+(5*6)+(4*1)+(3*3)+(2*3)+(1*8)=142
142 % 10 = 2
So 76613-38-2 is a valid CAS Registry Number.

76613-38-2Downstream Products

76613-38-2Relevant academic research and scientific papers

Thiadiaziridine 1,1-Dioxides: Synthesis and Chemistry

Timberlake, Jack W.,Alender, Jeff,Garner, Archie W.,Hodges, Melvin L.,Oezmeral, Cenan,et al.

, p. 2082 - 2089 (2007/10/02)

The synthesis and chemical reactions of a series of thiadiaziridine 1,1-dioxides (2) are described.The thermal stability is highly dependent on the R group and in one case (R = tert-octyl) is postulated that the thermolysis initially produces a diradical intermediate which can be trapped or further fragments to give a nitrene.A temperature-dependent NMR study on the coalescence of the diastereotopic α-methyl protons of 2b gives a ΔG = 20 kcal*mol-1.

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