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tert-butyl 5-cyanospiro[3H-fur

o[2,3-c]pyridine-2,4'-piperidine]-1'-carboxylate,2771352-84-0,≥97%,阿拉丁
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  • T679415
  • 2026年01月06日
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 保存条件

      2-8°C储存

    • 英文名

      tert-butyl 5-cyanospiro[3H-furo[2,3-c]pyridine-2,4'-piperidine]-1'-carboxylate

    • 库存

      期货

    • 供应商

      上海阿拉丁生化科技股份有限公司

    • CAS号

      2771352-84-0

    • 规格

      T679415-1g

    中文名:tert-butyl 5-cyanospiro[3H-furo[2,3-c]pyridine-2,4'-piperidine]-1'-carboxylate
    英文名:tert-butyl 5-cyanospiro[3H-furo[2,3-c]pyridine-2,4'-piperidine]-1'-carboxylate
    纯度或规格:≥97%
    SPU:T679415
    CAS:2771352-84-0
    存储温度:2-8°C储存
    运输条件:低温运输
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    图标文献和实验
    相关实验
    • RNA Synthesis Using 2-O-(Tert-Butyldimethylsilyl) Protection

      This chapter enables the reader to carry out the solid-phase synthesis of ribonucleic acid (RNA) using β-cyanoethyl phosphoramidite chemistry combined with tert -butyldimethylsilyl protection of the ribose 2′-hydroxyl group. Phosphoramidite

    • Synthesis of Peptides Using Tert-Butyloxycarbonyl (Boc) as the -Amino Protection Group

      The use of the tert -butyloxycarbonyl (Boc) as the N α-amino protecting group in peptide synthesis can be advantageous in several cases, such as synthesis of hydrophobic peptides and peptides containing ester and thioester moieties

    • Two dimensional peptide mapping

      will probably go down. After exposure, cut out the membrane piece of interest and soak it immediately in 0.5% PVP-360 (Polyvinylpyrrolidone, MW360) in 100mM acetic acid for 30 min. at 37°C. If you don't do this, your yield will be poor. This may result

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