15525
Boc-Tyr-OSu
≥99.0% (N)
别名:
Boc-L-酪氨酸羟基琥珀酰亚胺酯
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关于此项目
经验公式（希尔记法）:
C18H22N2O7
化学文摘社编号:
分子量:
378.38
PubChem Substance ID:
UNSPSC Code:
12352200
Beilstein/REAXYS Number:
1557147
MDL number:
SMILES string
CC(C)(C)OC(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)ON2C(=O)CCC2=O
InChI
1S/C18H22N2O7/c1-18(2,3)26-17(25)19-13(10-11-4-6-12(21)7-5-11)16(24)27-20-14(22)8-9-15(20)23/h4-7,13,21H,8-10H2,1-3H3,(H,19,25)/t13-/m0/s1
InChI key
NZUDTLHVKHXJJJ-ZDUSSCGKSA-N
assay
≥99.0% (N)
optical activity
[α]20/D −13±1°, c = 1% in dioxane
mp
~190 °C (dec.)
application(s)
peptide synthesis
storage temp.
−20°C
Other Notes
用于肽的碘代酪氨酰化反应快速方法的试剂。；该方法与 Bolton-Hunter 方法相同，但是具有其他优点，衍生肽容易解块形成放射性标记产物，与原料具有相同的净电荷。
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
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R K Assoian et al.
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International journal of pharmaceutics, 566, 141-148 (2019-05-28)
Small interfering RNAs (siRNAs) can down-regulate the expression of a target mRNA molecule in a sequence-specific manner, making them an attractive new class of drugs with broad potential for the treatment of diverse human diseases. Here, we report the synthesis
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