263826
4-Iodobenzaldehyde
96%
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About This Item
Linear Formula:
IC6H4CHO
CAS Number:
Molecular Weight:
232.02
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
InChI
1S/C7H5IO/c8-7-3-1-6(5-9)2-4-7/h1-5H
SMILES string
Ic1ccc(C=O)cc1
InChI key
NIEBHDXUIJSHSL-UHFFFAOYSA-N
assay
96%
mp
78-82 °C (lit.)
functional group
aldehyde, iodo
storage temp.
2-8°C
Quality Level
General description
4-Iodobenzaldehyde participates in Suzuki–Miyaura coupling reaction to produce Metal–Organic Framework catalyst.
Application
4-Iodobenzaldehyde has been used in the preparation of:
- benzaldimine monolayers
- 4-[2-(trimethylsilyl)ethynyl]benzaldehyde
- 5,15-dimesityl-10-(3-[2-(trimethylsilyl)ethynyi]phenyl}-20-(4-iodophenyl)porphyrin
- 5,15-dimesityl-10-[3,5-bis{2-[4-(N,N′-difluoroboryl-1,9-dimethyidipyrrin-5-yl)-phenyl]ethynyl}phenyl]-20-(4-iodophenyl)porphyrin, multipigment building block
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Amino-Induced 2D Cu-Based Metal--Organic Framework as an Efficient Heterogeneous Catalyst for Aerobic Oxidation of Olefins
Tang J, et al.
Chemistry?A European Journal , 26, 4333-4340 (2020)
Selective cleavage of the carbon-halide bond in substituted benzaldimine monolayers by synchrotron soft X-ray: Anomalously large cleavage rate of the carbon-bromide bond.
Moon JH, et al.
Langmuir, 16(6), 2981-2984 (2000)
Trans-Substituted porphyrin building blocks bearing iodo and ethynyl groups for applications in bioorganic and materials chemistry.
Ravikanth M, et al.
Tetrahedron, 54(27), 7721-7734 (1998)
Umar Ali Dar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 240, 118570-118570 (2020-06-27)
The current study determines optical and fluorescence response of halogen substituted series of meso‑tetrakis‑(4‑halophenyl) porphyrin; H2TXPP (Halo = F, Cl, Br, I) dye in tetrahydrofuran; THF and THF-water system at changing pH in relationship with changing medium of allure. Effects produced
Abel T Demissie et al.
Journal of the American Chemical Society, 137(27), 8819-8828 (2015-06-23)
We report the systematic characterization of anisotropic, π-conjugated oligophenyleneimine (OPI) films synthesized using stepwise imine condensation, or "click" chemistry. Film synthesis began with a self-assembled monolayer (SAM) of 4-formylthiophenol or 4-aminothiophenol on Au, followed by repetitive, alternate addition of terephthalaldehyde
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