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Merck

55262

Sigma-Aldrich

4-[4-(1-羟乙基)-2-甲氧基-5-硝基苯氧基]丁酸

≥98.0% (HPLC), for peptide synthesis

别名:

羟乙基光偶联剂

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About This Item

经验公式(希尔记法):
C13H17NO7
分子量:
299.28
Beilstein:
7717635
MDL號碼:
分類程式碼代碼:
12352106
PubChem物質ID:
NACRES:
NA.22

product name

4-[4-(1-羟乙基)-2-甲氧基-5-硝基苯氧基]丁酸, ≥98.0% (HPLC)

化驗

≥98.0% (HPLC)

形狀

powder

反應適用性

reagent type: cross-linking reagent

mp

163-166 °C

SMILES 字串

COc1cc(C(C)O)c(cc1OCCCC(O)=O)[N+]([O-])=O

InChI

1S/C13H17NO7/c1-8(15)9-6-11(20-2)12(7-10(9)14(18)19)21-5-3-4-13(16)17/h6-8,15H,3-5H2,1-2H3,(H,16,17)

InChI 密鑰

DUIJUTBRRZCWRD-UHFFFAOYSA-N

其他說明

光敏交联剂,可键合到氨基及羟甲基树脂。用于合成敏感酸

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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D.L. Whitehouse et a
Tetrahedron Letters, 38, 7851-7851 (1997)
Christopher P. Holmes
The Journal of organic chemistry, 62(8), 2370-2380 (1997-04-18)
Both a model phenacyl and o-nitrobenzyl photolabile linker from the literature along with four new o-nitrobenzyl linkers were prepared and the kinetics of their photolytic cleavage examined in solution. The linkers were prepared by amidation of the carboxylic acid anchoring
Mime Kobayashi et al.
Journal of biomaterials science. Polymer edition, 30(13), 1161-1171 (2019-06-16)
We have developed biocompatible scaffolds that enable cell fate control with visible light. The scaffolds are based on synthetic collagen-like polypeptide, poly(prolyl-hydroxyprolyl-glycyl) {poly(Pro-Hyp-Gly)} which has been used for cosmetics and other healthcare applications. Bioactive peptides were conjugated to the scaffolds

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