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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-methylthiazol-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:
848472-61-7
- 规格:
T683152-5g/T683152-500mg/T683152-250mg/T683152-1g/T683152-10g/T683152-100mg
| 规格: | T683152-5g | 产品价格: | ¥38400.9 |
|---|---|---|---|
| 规格: | T683152-500mg | 产品价格: | ¥8528.9 |
| 规格: | T683152-250mg | 产品价格: | ¥5120.9 |
| 规格: | T683152-1g | 产品价格: | ¥12800.9 |
| 规格: | T683152-10g | 产品价格: | ¥64000.9 |
| 规格: | T683152-100mg | 产品价格: | ¥3072.9 |
英文名:tert-butyl N-(2-methylthiazol-4-yl)carbamate
纯度或规格:≥97%
SPU:T683152
CAS:848472-61-7
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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