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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 rel-(1R,2R,5S)-2-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate
- 库存:
期货
- 供应商:
上海阿拉丁生化科技股份有限公司
- 规格:
T681820-5g/T681820-500mg/T681820-25g/T681820-250mg/T681820-1g/T681820-10g/T681820-100mg
| 规格: | T681820-5g | 产品价格: | ¥22320.9 |
|---|---|---|---|
| 规格: | T681820-500mg | 产品价格: | ¥4752.9 |
| 规格: | T681820-25g | 产品价格: | ¥72000.9 |
| 规格: | T681820-250mg | 产品价格: | ¥2880.9 |
| 规格: | T681820-1g | 产品价格: | ¥7200.9 |
| 规格: | T681820-10g | 产品价格: | ¥37952.9 |
| 规格: | T681820-100mg | 产品价格: | ¥1808.9 |
英文名:tert-butyl rel-(1R,2R,5S)-2-(hydroxymethyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate
纯度或规格:≥97%
SPU:T681820
CAS:-
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
Detection of Aromatic -Hydroxyketones with Tetrazolium Salts
synthesis of the α-glucosidase inhibitor miglitol ([2R ,3R ,4R ,5S ]-1-[2-hydroxyethyl]-2-[hydroxymethyl]-3,4,5-piperidintriole) (1 ). Alternatively, thiamine diphosphate dependent transketolases are capable of synthesizing α-hydroxyketones by catalyzing
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