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关于此项目
经验公式(希尔记法):
C23H27NO5
化学文摘社编号:
分子量:
397.46
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
276-261-1
MDL number:
Beilstein/REAXYS Number:
4581133
产品名称
Fmoc-Thr(tBu)-OH, ≥98.0% (HPLC)
Quality Level
assay
≥98.0% (HPLC)
optical activity
[α]20/D +16±1°, c = 1% in ethyl acetate
reaction suitability
reaction type: C-H Activation, reaction type: Fmoc solid-phase peptide synthesis, reagent type: ligand
reaction type: Peptide Synthesis
application(s)
peptide synthesis
functional group
Fmoc, amine, carboxylic acid
storage temp.
2-8°C
SMILES string
C[C@@H](OC(C)(C)C)[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI
1S/C23H27NO5/c1-14(29-23(2,3)4)20(21(25)26)24-22(27)28-13-19-17-11-7-5-9-15(17)16-10-6-8-12-18(16)19/h5-12,14,19-20H,13H2,1-4H3,(H,24,27)(H,25,26)/t14-,20+/m1/s1
InChI key
LZOLWEQBVPVDPR-VLIAUNLRSA-N
General description
Fmoc-Thr(tBu)-OH也称为Fmoc-O-叔丁基-L-苏氨酸,常用作多肽合成中的氨基酸合成砌块。
Application
Fmoc-Thr(tBu)-OH可用于通过固相多肽合成反应合成chlorofusin类似物。此外,在复杂的缩酚酸肽(depsipeptide)固相合成中,可作为胺和羟基的保护基。
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
General Fmoc-Based Solid-Phase Synthesis of Complex Depsipeptides Circumventing Problematic Fmoc Removal
A Lobo-Ruiz
European Journal of Organic Chemistry, 2020, 183-192 (2020)
Solid-phase synthesis of chlorofusin analogues
ECY Woon
The Journal of Organic Chemistry, 72, 5146-5151 (2007)
Gizella Csire et al.
Journal of inorganic biochemistry, 203, 110927-110927 (2019-12-07)
Interaction of copper(II) and nickel(II) ions with the Ac-PHAAAGTHSMKHM-NH2 tridecapeptide containing the His85, His96 and His111 binding sites of human prion protein has been studied by various techniques. pH-potentiometry, UV-Vis and circular dichroism spectroscopy were applied to study the stoichiometry
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 47622-1KG-F | 04061826222676 |
| 47622-100G-F | 04061832362168 |
| 47622-25G-F | 04061832642550 |
| 47622-10G-F | 04061832362175 |
| 47622-1G-F | 04061826222669 |