叔丁基((3R,4S)-4-羟基四氢呋喃-3-基)氨基甲酸酯
tert-butyl((3R,4S)-4-hydroxytetrahydrofuran-3-yl)carbamate 1430230-65-1 **科研现货速达** ≥98% HPLC 随货提供COA、HPLC谱图、MS谱图，NMR图谱等，详细联系客服。用于LC-MS/MS定量分析，代谢组学、质谱，药代动力学等- 询价
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- 2025年08月09日
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
tert-butyl((3R,4S)-4-hydroxytetrahydrofuran-3-yl)carbamate
- 库存：
999
- 供应商：
智溯科ZSK
- CAS号：
1430230-65-1
- 规格：
10mg///100mg///200mg
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文献和实验. GC-MS methods based on the conversion into tert -butyldimethylsilyl (33 ) and N(O,S)-propoxycarbonyl propyl ester (34 ) derivatives, and LC-MS method were highly sensitive and specific, but these methods require expensive equipment. Furthermore, CZE
Synthesis of Peptidomimetic Conjugates of Cyclic Nucleoside Phosphonates
to 200 mesh, 1% cross‐linked, typical loading 1.0 to 1.8 mmol/g; Aldrich) Methyl O‐[tert‐butyl(dimethyl)silyl]‐(L )‐serinate ( S.6 a , see protocol
Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
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