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- 2026年05月08日
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- 库存：
期货
- 规格：
T669625-100mg/T669625-25mg
| 规格： | T669625-100mg | 产品价格： | ¥345.90 |
|---|---|---|---|
| 规格： | T669625-25mg | 产品价格： | ¥115.90 |
中文名：tert-butyl N-(methylcarbamothioyl)carbamate
英文名：tert-butyl N-(methylcarbamothioyl)carbamate
货号：T669625
Cas号：887913-52-2
存储温度：室温
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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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