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Merck
CN

15118

双(4-硝基苯)碳酸酯

purum, ≥97.0% (CHN)

别名:

4-硝基苯基碳酸酯

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关于此项目

线性分子式:
(O2NC6H4O)2CO
化学文摘社编号:
分子量:
304.21
EC Number:
225-775-4
UNSPSC Code:
12352108
PubChem Substance ID:
Beilstein/REAXYS Number:
1892897
MDL number:
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grade

purum

assay

≥97.0% (CHN)

mp

136-139 °C (lit.), 137-142 °C

SMILES string

[O-][N+](=O)c1ccc(OC(=O)Oc2ccc(cc2)[N+]([O-])=O)cc1

InChI

1S/C13H8N2O7/c16-13(21-11-5-1-9(2-6-11)14(17)18)22-12-7-3-10(4-8-12)15(19)20/h1-8H

InChI key

ACBQROXDOHKANW-UHFFFAOYSA-N

Application

合成氨基酸的 4-硝基苯基活性酯的试剂。用于制备对称和不对称脲。

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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A divalent knottin containing two separate integrin binding epitopes (RGD) in the adjacent loops, 3-4A, was recently developed and reported in our previous publication. In the current study, 3-4A was radiofluorinated with a 4-nitrophenyl 2-(18)F-fluoropropinate ((18)F-NFP) group and the resulting
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A general method for the preparation of bis-ureas from bis(o-nitrophenyl) carbonate has been developed. Directional urea synthesis is achieved by sequential amine addition to bis(o-nitrophenyl) carbonate in two steps: in the first step bis(o-nitrophenyl) carbonate is reacted with benzylamine to
G Cavallaro et al.
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