156241-41-7 Usage
Uses
Used in Chemical Synthesis:
HEXAFLUOROISOPROPYL TRIFLUOROMETHANESULFONATE is used as a chemical reagent in various organic synthesis processes, contributing to the creation of a wide range of specialty chemicals and materials.
Used in Electroplating Industry:
In the electroplating industry, HEXAFLUOROISOPROPYL TRIFLUOROMETHANESULFONATE serves as an additive, enhancing the quality and performance of the electroplated coatings.
Used in Electronic Components Manufacturing:
HEXAFLUOROISOPROPYL TRIFLUOROMETHANESULFONATE is utilized as a solvent and surface treatment agent in the manufacturing of electronic components, improving the performance and reliability of these components.
Used in Polymer Production:
HEXAFLUOROISOPROPYL TRIFLUOROMETHANESULFONATE is also used in the production of polymers, where its unique properties contribute to the development of advanced materials with specific characteristics for various applications.
Used in Specialty Chemicals Production:
HEXAFLUOROISOPROPYL TRIFLUOROMETHANESULFONATE is employed in the production of specialty chemicals, leveraging its thermal stability and low reactivity to create high-quality end products for diverse industries.
Check Digit Verification of cas no
The CAS Registry Mumber 156241-41-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,2,4 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 156241-41:
(8*1)+(7*5)+(6*6)+(5*2)+(4*4)+(3*1)+(2*4)+(1*1)=117
117 % 10 = 7
So 156241-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C4HF9O3S/c5-2(6,7)1(3(8,9)10)16-17(14,15)4(11,12)13/h1H
156241-41-7Relevant academic research and scientific papers
Conformational Equilibria due to Ring Inversion in N-Alkyl-cis-decahydroisoquinolines
Bailey, Judith M.,Booth, Harold,Al-Shirayda, Hatif A. R. Y.
, p. 583 - 588 (2007/10/02)
The position of conformational equilibria due to ring inversion in N-alkyl-cis-decahydroisoquinolines (alkyl = Me, Et, Pri, CH2CF3, or CH2CCl3) has been assessed directly from 13C and/or 19F n.m.r. spectra recorded at temperatures between 173 and 253 K.The measured equilibrium constants are related to the inductive effect of the N-substituent which produces an increase (Me, Et, Pri) or decrease (CH2CF3, CH2CCl3) in the magnitude of the gauche propylamine-type repulsive interaction. 13C Chemical shifts are tabulated for the carbon atoms of the two twin-chair conformations undergoing exchange.
