47623
Fmoc-Tyr(tBu)-OH
≥98.0% (HPLC), for peptide synthesis
别名:
N-(9-芴甲氧羰基)-O-叔丁基-L-酪氨酸, Fmoc-O-叔丁基-L-酪氨酸
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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)
InChI key
JAUKCFULLJFBFN-VWLOTQADSA-N
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
SMILES string
CC(C)(C)Oc1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)cc1
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
Quality Level
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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。
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。
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)
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