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- 英文名：
tert-Butyl N-(3,3,3-Trifluoro-2-hydroxypropyl)carbamate
- 库存：
100+
- 供应商：
上海维亦特生物
- CAS号：
1219606-48-0
tert-Butyl N-(3,3,3-Trifluoro-2-hydroxypropyl)carbamate
1219606-48-0
C₈H₁₄NO₃F₃
229.19
No Data Available
No Data Available
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文献和实验tert-Butyl N-(3,3,3-Trifluoro-2-hydroxypropyl)carbamate
1219606-48-0
C₈H₁₄NO₃F₃
229.19
No Data Available
No Data Available
Over the past 20 years, amino acid analysis methods based on precolumn derivatization procedures have become a popular alternative to the traditional postcolumn derivatization techniques based on ion-exchange separation of the underivatized
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
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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