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
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选择尺寸
关于此项目
经验公式（希尔记法）:
C17H16N4O3
化学文摘社编号:
分子量:
324.33
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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
SMILES string
C[C@H](NC(OCC1=CC=CC=C1)=O)C(N(N=N2)C3=C2C=CC=C3)=O
InChI key
LREHLGSLFLKDDH-LBPRGKRZSA-N
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
95-100 °C
application(s)
peptide synthesis
storage temp.
−20°C
Application
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
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_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
Katritzky, A. R.; et al.
The Journal of Organic Chemistry, 8690-8694 (2009)
Hansen, F. K.; et al.
Heterocycles, 515-526 (2012)
Abdelmajeid, A.; et al.
Synthesis, 2995-3005 (2011)
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