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
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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
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
产品名称
Fmoc-leu-bt, 97%
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
SMILES string
CC(C)C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(=O)n4nnc5ccccc45
InChI key
ZWFTXRDNFPCOSI-DEOSSOPVSA-N
assay
97%
form
solid
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
121-126 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°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
13 - Non 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
Abdelmajeid, A.; et al.
Synthesis, 2995-3005 (2011)
Hansen, F. K.; et al.
Heterocycles, 515-526 (2012)
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)
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