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- 文献和实验
- 技术资料
- 库存:
期货
- 英文名:
tert-butyl N-(3-acetylpyridin-4-yl)carbamate
- CAS号:
1620955-61-4
- 供应商:
上海阿拉丁生化科技股份有限公司
- 保存条件:
室温;常规运输
- 规格:
T1227654-100mg/T1227654-1g/T1227654-250mg/T1227654-500mg/T1227654-50mg
| 规格: | T1227654-100mg | 产品价格: | ¥4676.90 |
|---|---|---|---|
| 规格: | T1227654-1g | 产品价格: | ¥12726.90 |
| 规格: | T1227654-250mg | 产品价格: | ¥6489.90 |
| 规格: | T1227654-500mg | 产品价格: | ¥10003.90 |
| 规格: | T1227654-50mg | 产品价格: | ¥3269.90 |
中文名:tert-butyl N-(3-acetylpyridin-4-yl)carbamate
英文名:tert-butyl N-(3-acetylpyridin-4-yl)carbamate
纯度:≥95%
货号:T1227654
Cas号:1620955-61-4
存储温度:室温
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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