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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
4-Methyl-piperidine-4-carboxylic acid amide hydrochloride
- 库存:
999
- 供应商:
智溯科ZSK
- CAS号:
1257301-28-2
- 规格:
10mg///100mg///200mg
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文献和实验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
Disulfide Conjugation of Peptides to Oligonucleotides and Their Analogs
‐Diisopropylethylamine (DIPEA, 99+%, Applied Biosystems) Piperidine (>99.5%, Romil) NovaSyn TGR resin (for C‐terminal amide synthesis
Uridine 2′‐Carbamates: Facile Tools for Oligonucleotide 2′‐Functionalization
1‐Pyrenemethylamine hydrochloride (Aldrich; for S.4d ) 2‐Aminomethyl‐15‐crown‐5 (for S.4e )
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