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Jms s3000 spiraltof plus 2

Manufactured by JEOL
Sourced in Japan

The JMS-S3000 SpiralTOFTM-plus 2.0 is a high-performance mass spectrometer developed by JEOL. It features a spiral-type time-of-flight (TOF) analyzer, providing high mass resolution and mass accuracy. The instrument is designed for various analytical applications that require precise mass determination and high-throughput analysis.

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2 protocols using jms s3000 spiraltof plus 2

1

Purification and Characterization of Novel Compounds

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The starting materials, reagents, and solvents were purchased from Tokyo Chemical Industry Co., Ltd. (Tokyo, Japan), FUJIFILM Wako Pure Chemical Corporation (Osaka, Japan), Kanto Chemical Co., Inc. (Tokyo, Japan) and Sigma-Aldrich (Tokyo, Japan), and used without further purification. Silica gel 70 F254 TLC plates (FUJIFILM Wako, Osaka, Japan) were used for analytical Tin-layer chromatography (TLC), while Silica gel 60 N (spherical, neutral, Kanto Chemical (Tokyo, Japan)) was for column chromatography. For preparative flash chromatography, used was an automated system (Smart Flash EPCLC AI-580S, Yamazen Corp., Osaka, Japan) equipped with universal columns of silica gel. 1H and 13C NMR spectra were determined with a JEOL ECA-500 instrument (500 MHz for 1 H and 126 MHz for 13C) (JEOL, Tokyo, Japan). Mass spectra were obtained with a high-resolution electrospray ionization mass spectrum (JMS-T100LC) (JEOL, Tokyo, Japan) and Matrix-assisted laser desorption/ionization mass spectrum (JMS-S3000 SpiralTOFTM-plus 2.0) (JEOL, Tokyo, Japan).
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2

Synthetic Strategies for Novel Heterocyclic Compounds

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The starting materials, reagents, and solvents were purchased from Tokyo Chemical Industry Co., Ltd., FUJIFILM Wako Pure Chemical Corporation, Kanto Chemical Co., Inc., and Sigma-Aldrich, and were used without further purification. Silica gel 70 F254 TLC plates (Wako) were used for analytical thin-layer chromatography (TLC), whereas Silica gel 60 N (spherical, neutral; Kanto Chemical) was applied in column chromatography. For preparative flash chromatography, an automated system (Smart Flash EPCLC AI-580S; Yamazen Corp., Japan) equipped with universal columns of silica gel was used. The 1H and 13C NMR spectra were determined using a JEOL ECA-500 instrument (500 MHz for 1 H and 126 MHz for 13C). Mass spectra were obtained with a high-resolution electrospray ionization mass spectrometer (JMS-T100LC; JEOL) and a matrix-assisted laser desorption/ionization mass spectrometer (JMS-S3000 SpiralTOFTM-plus 2.0; JEOL).
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