叔丁基6-氰基-2-(2-(4-乙基-3-碘苯基)丙-2-基
)-1H-吲哚-3-羧酸酯 tert-Butyl6-cyano-2-(2-(4-ethyl-3-iodophenyl)propan-2-yl)-1H-indole-3-carboxylate 1256584-75-4 **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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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
tert-Butyl6-cyano-2-(2-(4-ethyl-3-iodophenyl)propan-2-yl)-1H-indole-3-carboxylate
- 库存：
999
- 供应商：
智溯科ZSK
- CAS号：
1256584-75-4
- 规格：
10mg
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文献和实验and lack sensitivity. GC methods based on the conversion into trimethylsilyl (4 ,5 ), neopentylidine (6 ), and N-trifluoroacetyl n -butyl ester (7 ) derivatives lack sensitivity, gives a tailing peak and requires anhydrous derivatization conditions
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
Enzymes Acting on d-Amino Acid Containing Peptides
aminopeptidase and endopeptidase activities. The enzyme was active toward (d -Phe) n , Boc-(d -Phe) n , (d -Phe) n methyl ester, d -Phe-NH2 , Boc-(d -Phe) n methyl ester, and Boc-(d -Phe) n tert -butyl ester, but not toward (d -Ala) n (n = 2–4), (d
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