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- PBZS8042
- 2025年07月15日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Recommended Refrigeration Conditions (2℃-8℃) for storage
- 英文名：
3-(boc-amino)-2-(trifluormethyl)piperidine
- 供应商：
南京鼎石
- CAS号：
1824347-45-6
- 规格：
10g///25g///50g///100g///250g///500g///1kg///5kg///13139kg
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文献和实验Characterization of Wild‐Type Excitatory Amino Acid Ion Channel Receptors
3 H‐labeled radioligand (NEN Life Sciences): e.g., [3 H]D‐(−)‐3‐(2‐carboxy‐piperazine‐ 4‐yl)propyl‐1‐phosphonic acid ([3 H]CPP); [3 H]‐(±)‐cis ‐4‐phosphono‐methyl‐2‐piperidine carboxylic acid ([3 H]CGS 19755); or [3 H](±)‐E ‐2‐amino
Synthesis and Probing of Membrane-bound Peptide Arrays
should be Cys(Acm) or Cys(Trt), Asp(OtBu), Glu(OtBu), His(Trt), Lys(Boc), Asn(Trt), Gln(Trt), Arg(Pmc), Ser(tBu), Thr(tBu), Trp(Boc), and Tyr(tBu). HOBt-esters of these amino acid derivatives must be prepared in NMP for use throughout in spotting reactions
Solid-Phase Synthesis of Neuropeptides by Fmoc Strategies
is used to protect the α-amino group of each residue. Those residues that have potentially reactive side chains are protected with acid-labile groups such as t-butyl. After removal of the Fmoc group with piperidine, the next protected amino
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