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- 详细信息
- 文献和实验
- 技术资料
- 库存:
期货
- 规格:
T669606-25mg/T669606-5mg
| 规格: | T669606-25mg | 产品价格: | ¥1344.90 |
|---|---|---|---|
| 规格: | T669606-5mg | 产品价格: | ¥384.90 |
中文名:tert-butyl N-methyl-N-(4-nitrophenyl)carbamate
英文名:tert-butyl N-methyl-N-(4-nitrophenyl)carbamate
货号:T669606
Cas号:474020-88-7
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
and lack sensitivity. GC methods based on the conversion into trimethylsilyl (4 ,5 ), neopentylidine (6 ), and N-trifluoroacetyl n -butyl ester (7 ) derivatives lack sensitivity, gives a tailing peak and requires anhydrous derivatization conditions
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