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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
tert-butyl N-(6-aminopyridin-3-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:
445432-37-1
- 规格:
T633902-500mg/T633902-250mg/T633902-1g/T633902-100mg
| 规格: | T633902-500mg | 产品价格: | ¥3607.9 |
|---|---|---|---|
| 规格: | T633902-250mg | 产品价格: | ¥1812.9 |
| 规格: | T633902-1g | 产品价格: | ¥6526.9 |
| 规格: | T633902-100mg | 产品价格: | ¥979.9 |
设定黄金标准,在阿拉丁,我们不仅相信保持质量,而且相信质量。 我们的目标是定义它。 我们的质量管理理念为业界研究试剂建立了高质量的标准。 当您听到阿拉丁这个名字时,就会知道它是各个方面坚定不移品质的灯塔。
中文名:tert-butyl N-(6-aminopyridin-3-yl)carbamate
英文名:tert-butyl N-(6-aminopyridin-3-yl)carbamate
纯度:≥97%
cas号:445432-37-1
存储温度:-
运输条件:常规运输
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文献和实验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
N‐/purin‐6‐yl/pyridinium salts. Nucleic Acids Res. 13:2989‐3003. Allerson, C.R., Chen, S.L., and Verdine, G.L. 1997. A chemical method for site‐specific modification
and lack sensitivity. GC methods based on the conversion into trimethylsilyl (4 ,5 ), neopentylidine (6 ), and N-trifluoroacetyl n -butyl ester (7 ) derivatives lack sensitivity, gives a tailing peak and requires anhydrous derivatization conditions
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