Merck
CN
所有图片(2)

文件

411914

Sigma-Aldrich

3-硝基邻苯二腈

99%

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线性分子式:
O2NC6H3(CN)2
CAS号:
51762-67-5
分子量:
173.13
Beilstein:
2263686
MDL编号:
MFCD00191558
PubChem化学物质编号:
24865773
NACRES:
NA.47

质量水平

100

检测方案

99%

形式

solid

mp

162-165 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

储存温度

room temp

SMILES string

[O-][N+](=O)c1cccc(C#N)c1C#N

InChI

1S/C8H3N3O2/c9-4-6-2-1-3-8(11(12)13)7(6)5-10/h1-3H

InChI key

UZJZIZFCQFZDHP-UHFFFAOYSA-N

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相关类别

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Armağan Günsel et al.
Dalton transactions (Cambridge, England : 2003), 48(39), 14839-14852 (2019-09-26)
This study describes the synthesis and characterization of a non-peripherally tetra-substituted copper(ii) phthalocyanine bearing 4-(trifluoromethoxy)phenol groups. Some spectroscopic techniques such as FT-IR, 1H-NMR, 13C-NMR, MALDI-TOF, SEM and UV-vis were used to characterize the compounds. The novel molecule of 3-(4-(trifluoromethoxy) phenoxy)
G S Amitha et al.
Journal of fluorescence, 29(1), 279-291 (2019-01-10)
A novel 4,4'-fluoresceinoxy bisphthalonitrile FPN is synthesized from fluorescein and 4-nitrophthalonitrile by aromatic nucleophilic ipso nitro substitution reaction. The structure of FPN constitutes phthalonitrile-fluorescein-phthalonitrile, acceptor-donor-acceptor, A-D-A form and the solvatochromic study of newly synthesized compound FPN was done in hexane
Taner Arslan et al.
Journal of fluorescence, 30(2), 365-373 (2020-02-23)
In present work, a new substituted phthalonitrile derivative was prepared by the nucleophilic displacement reaction and then highly soluble zinc phthalocyanine (ZnPc) with four peripheral 1-hydroxyhexan-3-ylthio groups was synthesized by cyclotetramerization and characterized by FTIR, 1H and 13C NMRs spectroscopies
Min Wang et al.
Nature communications, 10(1), 3602-3602 (2019-08-11)
Molecular catalysts that combine high product selectivity and high current density for CO2 electrochemical reduction to CO or other chemical feedstocks are urgently needed. While earth-abundant metal-based molecular electrocatalysts with high selectivity for CO2 to CO conversion are known, they

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