tert-butyl 5-chlorospiro[3H-fu
ro[2,3-c]pyridine-2,4'-piperidine]-1'-carboxylate CAS号 1380537-63-2- ￥14859
- 维克奇生物
- 四川.成都
- WKQ-0870435
- 2025年11月27日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
储存条件：-20℃，干燥、避光、密封
- 保质期：
2年
- 英文名：
tert-butyl 5-chlorospiro[3H-furo[2,3-c]pyridine-2,4'-piperidine]-1'-carboxylate
- 库存：
1000
- 供应商：
四川省维克奇生物科技有限公司
- CAS号：
1380537-63-2
- 规格：
500mg
英文名称：tert-butyl 5-chlorospiro[3H-furo[2,3-c]pyridine-2,4'-piperidine]-1'-carboxylate
分子式：C16H21N2O3Cl
CAS：1380537-63-2
纯度：≥97%
储存条件：-20℃，干燥、避光、密封
规格：5mg10mg20mg50mg100mg500mg1g80g等应客户需求包装
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文献和实验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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