- 询价
- ITI Biochem
- 美国
- 73874-95-0
- 2025年07月17日
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![3-PHENYL-1-(PYRIDIN-2-YL)-6,7,8,9-TETRAHYDRO-5H-CYCLOHEPTA[C]PYRIDINE](https://img1.dxycdn.com/p/s14/2025/0228/055/0637678947310935981.jpg!wh200)
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
4-(Boc-amino)piperidine
- 库存：
98
- 供应商：
北京孚博
- CAS号：
73874-95-0
- 规格：
1g
CAS：73874-95-0
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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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