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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 N-[1-(azetidin-3-yl)ethyl]carbamate;hydrochloride
- 库存:
期货
- 供应商:
上海阿拉丁生化科技股份有限公司
- CAS号:
1379363-25-3
- 规格:
T681089-500mg/T681089-250mg/T681089-1g/T681089-100mg
| 规格: | T681089-500mg | 产品价格: | ¥9120.9 |
|---|---|---|---|
| 规格: | T681089-250mg | 产品价格: | ¥5472.9 |
| 规格: | T681089-1g | 产品价格: | ¥13680.9 |
| 规格: | T681089-100mg | 产品价格: | ¥4096.9 |
英文名:tert-butyl N-[1-(azetidin-3-yl)ethyl]carbamate;hydrochloride
纯度或规格:≥97%
SPU:T681089
CAS:1379363-25-3
存储温度:2-8°C储存
运输条件:低温运输
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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
Uracil‐1‐yl acetic acid (2 ; protocol 1 ) N ‐(2‐((tert ‐Butyldimethylsilyl)oxy)ethyl)prop‐2‐yn‐1‐amine (8 ; protocol
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