355-27-1 Usage
Uses
Used in Surface Modification Industry:
1H,1H-Nonafluoropentylamine is used as a surface modifying agent for imparting superhydrophobic properties to surfaces, which repels both water and oil. This characteristic is valuable in applications requiring non-stick or easy-to-clean surfaces.
Used in Fluoropolymer Production:
In the fluoropolymer industry, 1H,1H-Nonafluoropentylamine serves as a crucial component in the synthesis of fluoropolymers, contributing to the development of materials with enhanced chemical resistance and thermal stability.
Used as a Surfactant in Chemical Processes:
1H,1H-Nonafluoropentylamine is utilized as a surfactant in a range of chemical processes, where it helps to reduce surface tension and stabilize emulsions, facilitating various industrial processes.
Used in the Synthesis of Other Fluorinated Compounds and Materials:
1H,1H-Nonafluoropentylamine also functions as a building block in the creation of other fluorinated compounds and materials, expanding its applications across different sectors that require specialized fluorinated products.
Given the potential environmental and health risks associated with 1H,1H-Nonafluoropentylamine, its use and handling must be approached with caution, and safety protocols should be strictly followed to mitigate any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 355-27-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 355-27:
(5*3)+(4*5)+(3*5)+(2*2)+(1*7)=61
61 % 10 = 1
So 355-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H4F9N/c6-2(7,1-15)3(8,9)4(10,11)5(12,13)14/h1,15H2
355-27-1Relevant academic research and scientific papers
Biomimetic reductive amination under the continuous-flow reaction conditions
Soloshonok, Vadim A.,Catt, Hector T.,Ono, Taizo
body text, p. 261 - 265 (2010/04/05)
This study present a full account of continuous-flow reaction conditions for biomimetic reductive amination of fluorinated carbonyl compounds to corresponding amines and amino acids of biomedical importance. We demonstrate that simple silica-adsorbed DBU can be used as efficient catalysts for on-column 1,3-proton shift reaction, a key transformation in the biomimetic reductive amination process. This new on-column process features operationally convenient conditions, higher chemical yields, enantioselectivity and purity of the corresponding products as compared with traditional in-flask reactions. Moreover the removal of base-catalyst, the most delicate problem of the in-flask reactions, is not an issue in the on-column process, as the silica-adsorbed DBU or polymer-bound guanidine remains on the column and can be reused. This feature renders the overall process substantially more economical and synthetically efficient, in particular, for large-scale synthesis of the corresponding fluorinated amines and amino acids target.
