737798
Fmoc-leu-bt
97%
别名:
(S)-(9H-Fluoren-9-yl)methyl 1-(1H-benzo[d][1,2,3]triazol-1-yl)-4-methyl-1-oxopentan-2-ylcarbamate, (S)-N-Fmoc-1-benzotriazolylcarbonyl-3-methylbutylamine
登录查看公司和协议定价
选择尺寸
关于此项目
经验公式（希尔记法）:
C27H26N4O3
化学文摘社编号:
分子量:
454.52
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.26
方案
97%
表单
solid
反应适用性
reaction type: Fmoc solid-phase peptide synthesis
mp
121-126 °C
应用
peptide synthesis
官能团
Fmoc
储存温度
2-8°C
SMILES字符串
CC(C)C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(=O)n4nnc5ccccc45
InChI
1S/C27H26N4O3/c1-17(2)15-24(26(32)31-25-14-8-7-13-23(25)29-30-31)28-27(33)34-16-22-20-11-5-3-9-18(20)19-10-4-6-12-21(19)22/h3-14,17,22,24H,15-16H2,1-2H3,(H,28,33)/t24-/m0/s1
InChI key
ZWFTXRDNFPCOSI-DEOSSOPVSA-N
应用
Benzotriazole amino acids, or aminoacylbenzotriazolides, are versatile reagents for synthesizing peptides as well as their mimetics and conjugates. Benzotriazole amino acids have been used for the preparation of diverse derivatives including:
- Polypeptidal benzotriazolides
- Peptidomimetics, such as aminoxypeptides, depsipeptides and heterocyclic peptidomimetics
- Tagged peptides and peptidomimetics, particularly those with fluorescent labels,
- N, O, S, and C linked peptide conjugates
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
此项目有
Hansen, F. K.; et al.
Heterocycles, 515-526 (2012)
Abdelmajeid, A.; et al.
Synthesis, 2995-3005 (2011)
Katritzky, A. R.; et al.
Synlett, 2392-2411 (2009)
Katritzky, A. R.; et al.
The Journal of Organic Chemistry, 8690-8694 (2009)
Avan, I.; et al.
The Journal of Organic Chemistry, 4884-4893 (2011)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持