737747
z-ala-bt
别名:
(S)-N-Z-1-(Benzotriazolylcarbonyl)ethylamine, (S)-Benzyl 1-(1H-benzo[d][1,2,3] triazol-1-yl)-1-oxopropan-2-ylcarbamate
表单
solid
反应适用性
reaction type: solution phase peptide synthesis
mp
95-100 °C
应用
peptide synthesis
储存温度
−20°C
SMILES字符串
C[C@H](NC(OCC1=CC=CC=C1)=O)C(N(N=N2)C3=C2C=CC=C3)=O
InChI
1S/C17H16N4O3/c1-12(18-17(23)24-11-13-7-3-2-4-8-13)16(22)21-15-10-6-5-9-14(15)19-20-21/h2-10,12H,11H2,1H3,(H,18,23)/t12-/m0/s1
InChI key
LREHLGSLFLKDDH-LBPRGKRZSA-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
11 - 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
Katritzky, A. R.; et al.
Synlett, 2392-2411 (2009)
Avan, I.; et al.
The Journal of Organic Chemistry, 4884-4893 null
Abdelmajeid, A.; et al.
Synthesis, 2995-3005 (2011)
Katritzky, A. R.; et al.
The Journal of Organic Chemistry, 8690-8694 (2009)
Hansen, F. K.; et al.
Heterocycles, 515-526 (2012)
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