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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 N-(2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-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:
86499-69-6
- 规格:
T682966-5g/T682966-500mg/T682966-250mg/T682966-1g/T682966-10g/T682966-100mg
| 规格: | T682966-5g | 产品价格: | ¥8816.9 |
|---|---|---|---|
| 规格: | T682966-500mg | 产品价格: | ¥1968.9 |
| 规格: | T682966-250mg | 产品价格: | ¥1184.9 |
| 规格: | T682966-1g | 产品价格: | ¥2944.9 |
| 规格: | T682966-10g | 产品价格: | ¥14992.9 |
| 规格: | T682966-100mg | 产品价格: | ¥880.9 |
英文名:tert-butyl N-(2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-3-yl)carbamate
纯度或规格:≥97%
SPU:T682966
CAS:86499-69-6
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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