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关于此项目
经验公式(希尔记法):
C28H29NO5
化学文摘社编号:
分子量:
459.53
NACRES:
NA.26
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352209
EC Number:
276-262-7
MDL number:
Beilstein/REAXYS Number:
4216652
产品名称
Fmoc-Tyr(tBu)-OH, ≥98.0% (HPLC)
Quality Level
assay
≥98.0% (HPLC)
form
powder
optical activity
[α]20/D −29±2°, c = 1% in DMF
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
153-156 °C (lit.)
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
SMILES string
CC(C)(C)Oc1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)cc1
InChI
1S/C28H29NO5/c1-28(2,3)34-19-14-12-18(13-15-19)16-25(26(30)31)29-27(32)33-17-24-22-10-6-4-8-20(22)21-9-5-7-11-23(21)24/h4-15,24-25H,16-17H2,1-3H3,(H,29,32)(H,30,31)/t25-/m0/s1
InChI key
JAUKCFULLJFBFN-VWLOTQADSA-N
General description
Fmoc-Tyr(tBu)-OH也称为Fmoc-O-叔丁基-L-酪氨酸,通常用于Fmoc固相法肽合成。
Application
Fmoc-Tyr(tBu)-OH可用于通过水中固相反应合成亮氨酸-脑啡肽酰胺(Leu-Enkephalin Amide)。也用于合成氨基酸衍生物,例如Fmoc-Tyr-OAllyl。
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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)
Solid-Phase Total Synthesis of the Proposed Structure of Coibamide A and Its Derivative: Highly Methylated Cyclic Depsipeptides
GA Sable
European Journal of Organic Chemistry, 2015, 7043-7052 (2015)
Solid-phase peptide synthesis using nanoparticulate amino acids in water
K Hojo
Journal of Peptide Science, 13, 493-497 (2007)
Loay Awad et al.
Chembiochem : a European journal of chemical biology, 17(24), 2353-2360 (2016-10-28)
We present the design, synthesis, and characterization of a novel photocaged glutamine derivative (modified on the side chain of glutamine), and describe its use in enhancing peptide stability and solubility. Our results demonstrate that this approach can be used to
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 47623-10G-F | 04061832362199 |
| 47623-1KG-F | 04061826222683 |
| 47623-100G-F | 04061832362182 |
| 47623-25G-F | 04061832362205 |