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Merck
CN

515426

4-Iodophthalonitrile

97%

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About This Item

Linear Formula:
IC6H3-1,2-(CN)2
CAS Number:
Molecular Weight:
254.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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Product Name

4-Iodophthalonitrile, 97%

InChI

1S/C8H3IN2/c9-8-2-1-6(4-10)7(3-8)5-11/h1-3H

SMILES string

Ic1ccc(C#N)c(c1)C#N

InChI key

OOHQHYJZUSXMFD-UHFFFAOYSA-N

assay

97%

mp

140-142 °C (lit.)

functional group

iodo
nitrile

Quality Level

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - 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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Alkynyl substituted phthalocyanine derivatives as targets for optical limiting
Garcia-Frutos EM, et al.
Journal of Materials Chemistry, 13(4), 749-753 (2003)
Novel perfluoroalkyl phthalocyanine metal derivatives: Synthesis and photodynamic activities.
Qiu T, et al.
Dyes and Pigments, 83(1), 127-133 (2009)
Vibrational spectra of halophthalonitriles.
Halls MD, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 54(2), 305-317 (1998)
The synthesis of a fluorinated phthalocyanine.
Keller TM and Griffith JR.
Journal of Fluorine Chemistry, 13(1), 73-77 (1979)
Canan Uslan et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 24(2), 191-210 (2019-01-24)
Zinc(II) (5), indium(III) (6), and lutetium(III) (7) phthalocyanines (Pcs) peripherally substituted with poly (ethylene glycol) (PEG) monomethyl ether 2000 (PEGME-2000) blocks were synthesized via Sonogashira coupling reaction with high yields and their photophysical, photochemical and photobiological properties were investigated. We

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