おすすめの製品
アッセイ
96%
mp
185 °C (dec.) (lit.)
SMILES記法
CN(C)c1ccc(cc1)\N=N\c2ccc(cc2)S(Cl)(=O)=O
InChI
1S/C14H14ClN3O2S/c1-18(2)13-7-3-11(4-8-13)16-17-12-5-9-14(10-6-12)21(15,19)20/h3-10H,1-2H3/b17-16+
InChI Key
VTVWTPGLLAELLI-WUKNDPDISA-N
類似した製品をお探しですか? 訪問 製品比較ガイド
以下による置換
Journal of Chromatography. B, Biomedical Sciences and Applications, 621, 133-133 (1993)
Comparative and optimized dabsyl-amino acid analysis of synthetic phosphopeptides and glycopeptides.
L Gorbics et al.
Journal of chromatography. A, 676(1), 169-176 (1994-07-29)
The optimal conditions for amino acid analysis of phosphopeptides and N-acetylglucosamine- and N-acetylgalactosamine-containing glycopeptides were investigated by dabsyl-Cl derivatization and reversed-phase high-performance liquid chromatographic separation. By comparing the chromatographic behaviour of the dabsylated phosphoamino acids and dabsylated aminosugars on three
Journal of Chromatography. B, Biomedical Sciences and Applications, 613, 137-137 (1993)
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
製品に関するお問い合わせはこちら(テクニカルサービス)