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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
tert-butyl N-(1-methylpiperidin-4-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:
607372-93-0
- 规格:
T634201-5g/T634201-1g
| 规格: | T634201-5g | 产品价格: | ¥11299.9 |
|---|---|---|---|
| 规格: | T634201-1g | 产品价格: | ¥2545.9 |
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-(1-methylpiperidin-4-yl)carbamate
英文名:tert-butyl N-(1-methylpiperidin-4-yl)carbamate
纯度:≥97%
cas号:607372-93-0
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
Enzymes Acting on d-Amino Acid Containing Peptides
aminopeptidase and endopeptidase activities. The enzyme was active toward (d -Phe) n , Boc-(d -Phe) n , (d -Phe) n methyl ester, d -Phe-NH2 , Boc-(d -Phe) n methyl ester, and Boc-(d -Phe) n tert -butyl ester, but not toward (d -Ala) n (n = 2–4), (d
Natural Product Chemistry in Action: The Synthesis of Melatonin Metabolites K1 and K2
melatonin, the kynurenamines N1-acetyl-N2 -formyl-5-methoxykynurenine (K1 ) and N -acetyl-5-methoxykynurenamine (K2 ). The four key synthetic transformations involve (a) conversion of 4-methoxy aniline into the tert -butyl (4-methoxyphenyl)carbamate, (b
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