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Merck
CN

411914

3-Nitrophthalonitrile

99%

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About This Item

Linear Formula:
O2NC6H3(CN)2
CAS Number:
51762-67-5
Molecular Weight:
173.13
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
24865773
MDL number:
MFCD00191558
Beilstein/REAXYS Number:
2263686

Key Documents

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Product Name

3-Nitrophthalonitrile, 99%

InChI

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

SMILES string

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

InChI key

UZJZIZFCQFZDHP-UHFFFAOYSA-N

assay

99%

form

solid

mp

162-165 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBN8682V
MKBL4174V
MKBL4176V
MKBJ2975V
MKBG8688V

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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
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
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)
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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