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线性分子式:
IC6H3-1,2-(CN)2
化学文摘社编号:
分子量:
254.03
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
4-碘酞腈, 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
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
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
Alkynyl substituted phthalocyanine derivatives as targets for optical limiting
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Novel perfluoroalkyl phthalocyanine metal derivatives: Synthesis and photodynamic activities.
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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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