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Direct catalytic synthesis of ε-caprolactam from cyclohexanol using [n-C16H33N (CH3)3]H2PW12O40 as a catalyst - ScienceDirect
![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)
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
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Organic‐acid mediated bulk polymerization of ε‐caprolactam and its copolymerization with ε‐caprolactone - Sanchez‐Sanchez - 2016 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library
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Structure of activators used (a) N-benzoyl e-caprolactam and (b) N,N... | Download Scientific Diagram
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Impurity Formation in the Beckmann Rearrangement of Cyclohexanone Oxime to Yield ε-Caprolactam | Industrial & Engineering Chemistry Research
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Microorganisms | Free Full-Text | Epsilon-Caprolactam- and Nylon Oligomer-Degrading Bacterium Brevibacterium epidermidis BS3: Characterization and Potential Use in Bioremediation
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J. Compos. Sci. | Free Full-Text | Compensation of Water Influence on Anionic Polymerization of ε-Caprolactam: 1. Chemistry and Experiments
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