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515426

Sigma-Aldrich

4-Iodophthalonitrile

97%

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About This Item

Linear Formula:
IC6H3-1,2-(CN)2
CAS Number:
69518-17-8
Molecular Weight:
254.03
MDL number:
MFCD01863730
UNSPSC Code:
12352100
PubChem Substance ID:
24873819
NACRES:
NA.22

Assay

97%

mp

140-142 °C (lit.)

functional group

iodo
nitrile

SMILES string

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

InChI

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

InChI key

OOHQHYJZUSXMFD-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BGBC3271V
BGBB9961
BGBB6960
BGBB2681
MKAA2483

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Novel perfluoroalkyl phthalocyanine metal derivatives: Synthesis and photodynamic activities.
Qiu T, et al.
Dyes and Pigments, 83(1), 127-133 (2009)
Alkynyl substituted phthalocyanine derivatives as targets for optical limiting
Garcia-Frutos EM, et al.
Journal of Materials Chemistry, 13(4), 749-753 (2003)
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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