- ￥837
- 源叶
- 中国
- V29294-100mg
- 2025年10月27日
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![2-CHLORO-1-[1-(4-FLUOROBENZYL)-2,5-DIMETHYL-1H-PYRROL-3-YL]ETHANONE;790681-72-0;98%;V20373-100mg](https://img1.dxycdn.com/p/s14/2025/1027/131/2990871289947862891.jpg!wh200)
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
RT
- 英文名：
tert-butyl trans-N-(3-methylsulfanylcyclobutyl)carbamate
- 库存：
99
- 供应商：
上海源叶生物科技有限公司
- CAS号：
2639187-41-8
- 规格：
100mg
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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
hydrolysis and sample extraction with tert-butyl-methylether, the residue is derivatized with 1,1,1,3,3,3-hexafluoroisopropanol and analyzed by HRGC-MS (detection limit 0.1 �g/L urine).
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
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