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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-{3-amino-2,2-difluorobicyclo[1.1.1]pentan-1-yl}carbamate
- 库存:
期货
- 供应商:
上海阿拉丁生化科技股份有限公司
- CAS号:
2913177-38-3
- 规格:
T679170-500mg/T679170-250mg/T679170-1g/T679170-100mg
| 规格: | T679170-500mg | 产品价格: | ¥23472.9 |
|---|---|---|---|
| 规格: | T679170-250mg | 产品价格: | ¥14080.9 |
| 规格: | T679170-1g | 产品价格: | ¥35200.9 |
| 规格: | T679170-100mg | 产品价格: | ¥8448.9 |
英文名:tert-butyl N-{3-amino-2,2-difluorobicyclo[1.1.1]pentan-1-yl}carbamate
纯度或规格:≥97%
SPU:T679170
CAS:2913177-38-3
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
(HPLC) (9 –32 ), GC-mass spectrometry (GC-MS) (33 ,34 ), liquid chromatography-mass spectrometry (LC-MS) (35 ), and capillary zone electrophoresis (CZE) (36 –38 ). However, isotachophoresis and AAA methods are nonselective for sulfur amino acids
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