![A new procedure to obtain ε-caprolactam catalyzed by a guanidinium salt - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C7NJ03443A A new procedure to obtain ε-caprolactam catalyzed by a guanidinium salt - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C7NJ03443A](https://pubs.rsc.org/image/article/2017/NJ/c7nj03443a/c7nj03443a-s2_hi-res.gif)
A new procedure to obtain ε-caprolactam catalyzed by a guanidinium salt - New Journal of Chemistry (RSC Publishing) DOI:10.1039/C7NJ03443A
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Direct catalytic synthesis of ε-caprolactam from cyclohexanol using [n-C16H33N (CH3)3]H2PW12O40 as a catalyst - ScienceDirect
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Polymerization of ϵ‐Caprolactam to Nylon‐6 Catalyzed by Barium σ‐Borane Complex under Mild Condition - Bhattacharjee - 2019 - ChemCatChem - Wiley Online Library
![Structure of activators used (a) N-benzoyl e-caprolactam and (b) N,N... | Download Scientific Diagram Structure of activators used (a) N-benzoyl e-caprolactam and (b) N,N... | Download Scientific Diagram](https://www.researchgate.net/profile/Elena-Rusu-2/publication/236152648/figure/fig1/AS:717908200153091@1548174061603/Structure-of-activators-used-a-N-benzoyl-e-caprolactam-and-b-N-N_Q320.jpg)
Structure of activators used (a) N-benzoyl e-caprolactam and (b) N,N... | Download Scientific Diagram
![Impurity Formation in the Beckmann Rearrangement of Cyclohexanone Oxime to Yield ε-Caprolactam | Industrial & Engineering Chemistry Research Impurity Formation in the Beckmann Rearrangement of Cyclohexanone Oxime to Yield ε-Caprolactam | Industrial & Engineering Chemistry Research](https://pubs.acs.org/cms/10.1021/acs.iecr.7b03824/asset/images/large/ie-2017-03824y_0006.jpeg)
Impurity Formation in the Beckmann Rearrangement of Cyclohexanone Oxime to Yield ε-Caprolactam | Industrial & Engineering Chemistry Research
![169297-53-4 | ε-Caprolactam-d10 | Hexahydro-3,4,5,6,7-d5-2H-azepin-2-one-3,4,5,6,7-d5 | C₆HD₁₀NO | TRC 169297-53-4 | ε-Caprolactam-d10 | Hexahydro-3,4,5,6,7-d5-2H-azepin-2-one-3,4,5,6,7-d5 | C₆HD₁₀NO | TRC](https://www.trc-canada.com/prod-img/C175667.png)
169297-53-4 | ε-Caprolactam-d10 | Hexahydro-3,4,5,6,7-d5-2H-azepin-2-one-3,4,5,6,7-d5 | C₆HD₁₀NO | TRC
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J. Compos. Sci. | Free Full-Text | Compensation of Water Influence on Anionic Polymerization of ε-Caprolactam: 1. Chemistry and Experiments
![7336-15-4 | N-(β-Cyanoethyl)caprolactam | Hexahydro-2-oxo-1H-azepine-1-propanenitrile; N-(2-Cyanoethyl)-ε-caprolactam; N-(β-Cyanethyl)-ε-caprolactam; N-(β-Cyanethyl)-ξ-caprolactam; N-(β-Cyanoethyl)-ε-caprolactam | C9H14N2O | TRC 7336-15-4 | N-(β-Cyanoethyl)caprolactam | Hexahydro-2-oxo-1H-azepine-1-propanenitrile; N-(2-Cyanoethyl)-ε-caprolactam; N-(β-Cyanethyl)-ε-caprolactam; N-(β-Cyanethyl)-ξ-caprolactam; N-(β-Cyanoethyl)-ε-caprolactam | C9H14N2O | TRC](https://www.trc-canada.com/prod-img/C982310.png)