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Model 341

Manufactured by PerkinElmer
Sourced in Germany

The Model 341 is a high-precision analytical instrument designed for various laboratory applications. It features advanced optics and electronics to provide accurate and reliable measurements. The core function of the Model 341 is to perform precise quantitative analysis of samples through spectroscopic techniques.

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6 protocols using model 341

1

Specific Rotation Measurement Protocol

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Specific rotation values were measured with a Perkin Elmer Model 341 (Überlingen, Germany).
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2

Characterization of Organic Compounds

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A PerkinElmer Model 341 polarimeter was applied to measure optical rotations. ECD spectra were acquired using a Chirascan V100 spectropolarimeter. NMR data were recorded at 400 or 600 MHz (Bruker AVANCE). HRESIMS spectra were obtained on a ThermoFisher mass spectrometer (LTQ Orbitrap XL). Size-exclusion chromatography was conducted with Sephadex LH-20. Column chromatography (CC) was applied using silica gel which was produced by Anhui Liangchen Co., Ltd.
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3

Characterization of Organic Compounds

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Optical rotations were measured at ambient temperature for solution in CHCl3 with a Perkin–Elmer automatic polarimeter, Model 341. Melting points were measured on a Kofler hot stage. All reactions were monitored by thin-layer chromatography (TLC) on silica gel 60 coated glass slides. Spots were visualized by charring with 5% H2SO4 in ethanol, 1% ninhydrine in ethanol, or UV light, as required. Column chromatography was performed by elution from prepacked (Biotage, Inc.) columns of silica gel with a Isolera Flash Chromatograph (Biotage), the latter being connected to an external Evaporative Light Scattering Detector, Model 380-LC (Varian, Inc.). Nuclear Magnetic Resonance (NMR) spectra were measured at 600 MHz for 1H, and 150 MHz for 13C with Bruker Avance spectrometers. Solvent peaks were used as internal references relative to TMS for 1H and 13C chemical shifts (ppm). Assignments of NMR signals were made by homonuclear and heteronuclear two-dimensional correlation spectroscopy, run with software supplied with the spectrometers. Liquid Chromatography–Electron Spray-Ionization Mass Spectrometry (ESI-MS) was performed with a Hewlett–Packard 1100 MSD spectrometer. Solutions in organic solvents were dried with anhydrous Na2SO4, and concentrated at 40°C/2 kPa.
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4

Specific Rotation Measurement Protocol

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Specific rotation values were measured with a Perkin Elmer Model 341 (Überlingen, Germany).
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5

Optical and Spectral Characterization

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Optical rotations were recorded with a Perkin Elmer Model 341 polarimeter. Absorption spectra were recorded on a JASCO V-650 spectrophotometer in diluted solution by using spectrophotometric grade solvents. Electronic circular dichroism (ECD) was measured on a Jasco J-815 Circular Dichroism Spectrometer (IFR140 facility -Biosit-Université de Rennes
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6

Analytical Characterization of Organic Compounds

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Optical rotations were measured on a Perkin Elmer model 341 polarimeter (589 nm, 20 °C).
NMR data were performed in CD 3 OD on Bruker Avance 500. HRESIMS data were gained using a Micromass Q-TOF high-resolution mass spectrometer. Mass spectra were recorded in the positive-ion mode in the range m/z 100-2000, with a mass resolution of 20000 and an acceleration voltage of 0.7 kV. CC was carried out on HP-20 resin (Sigma Aldrich). Flash chromatography was conducted on a Grace Reveleris system equipped with dual UV and ELSD detection using Grace® cartridges (Silica gel or RP-C 18 ). HPLC separations were performed on a Dionex apparatus equipped with an ASI-100 autosampler, an Ultimate 3000 pump, a STH 585 column oven, a diode array detector UVD 340S and a Chromeleon software. A prepacked RP-C 18 column (Phenomenex 250 x 15 mm, Luna 5 µ) was used for semi-preparative HPLC. The eluting mobile phase consisted of H 2 O with TFA (0.0025%) and CH 3 CN with a flow rate of 5 mL/min and the chromatogram was monitored at 205 and 210 nm. TLC were carried out using silica gel 60 F 254 pre-coated aluminium plates (0.2 mm, Merck). Spots were visualized through developing agent (CHCl 3 :MeOH:H 2 O, 14:6:1) and chromogenic agent (50% aq. H 2 SO 4 ) subsequent heating.
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