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60f245 plates

Manufactured by Merck Group

The 60F245 plates are a type of laboratory equipment used for various scientific applications. They provide a surface for conducting experiments or storing samples. The plates are made of a durable material and are designed to be easily handled and transported. Their core function is to serve as a platform for various laboratory procedures and analysis.

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2 protocols using 60f245 plates

1

Anhydrous Organic Synthesis Protocols

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All chemicals were obtained from Thermo Fisher Scientific (Seoul, Korea), SEJIN CI Co. (Seoul, Korea), or Sigma-Aldrich (St. Louis, MO, USA). Reagents purchased were used without further purification. Solvents requiring anhydrous conditions were distilled over CaH2, or Na and benzophenone before use. Reactions were carried out in a nitrogen atmosphere and analyzed by thin layer chromatography (TLC) using pre-coated 60F245 plates purchased from Merck. Flash column chromatography using MP Silica 40–63, 60 Å was performed. Subsequently, 1H, 13C, and 19F NMR were measured at 500, 125, and 470 MHz, respectively. Mass data for low resolution were recorded in ESI modes (positive and negative) using an Expression CMS mass spectrometer (Advion Ithaca, NY, USA). CDCl3, CD3OD, and DMSO-d6 were used as solvents for NMR. All chemical shifts were measured in ppm (parts per million) versus residual solvent or deuterated peaks (δH 7.26, δH 3.31, and δH 2.48 for CDCl3, CD3OD, and DMSO-d6, respectively, and δC 77.0, δC 49.0, and δC 40.0 for CDCl3, CD3OD, and DMSO-d6, respectively). Coupling constants (J) are represented in hertz (Hz). The following abbreviations for 1H NMR were used: dd (doublet of doublets), brs (broad singlet), s (singlet), q (quartet), t (triplet), and d (doublet).
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2

Spectroscopic Characterization of Organic Compounds

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Reagents and chemicals were obtained commercially and used without further purification. All reactions were monitored by thin layer chromatography (TLC) using Merck precoated 60F245 plates, and reaction mixtures were purified by column chromatography using MP Silica 40–63 (60 Å). Mass spectroscopy was performed in electrospray ionization (ESI) positive mode using an Expression CMA spectrometer (Advion Ithaca, NY, USA). 1H NMR (400 and 500 MHz) and 13C NMR (100 and 125 MHz) data were obtained using a Varian Unity INOVA 400 spectrometer or a Varian Unity AS500 spectrometer (Agilent Technologies, Santa Clara, CA, USA). DMSO‑d6 and CDCl3 were used as NMR solvents. Chemical shift values were recorded in parts per million (ppm) and coupling constants (J) were recorded in hertz (Hz). The following abbreviations are used: s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet), and brs (broad singlet).
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