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Quality Level
Assay
98%
mp
27-29 °C (lit.)
SMILES string
Clc1ccc(I)cc1Cl
InChI
1S/C6H3Cl2I/c7-5-2-1-4(9)3-6(5)8/h1-3H
InChI key
NADPFZNWCQIJJW-UHFFFAOYSA-N
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General description
3,4-Dichloroiodobenzene undergoes Stille coupling reaction with vinyltributyltin in the presence of Pd(0)precursors to furnish styrene derivative.
Application
3,4-Dichloroiodobenzene may be used in the preparation of:
- tetrachloromethoxybiphenyls
- 1-(3,4-dichlorophenyl)-2-trimethylsilylacetylene
- 2-(3,4-dichlorocinnamyl)isoindoline-1,3-dione
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
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Synthesis and properties of various poly (diphenylacetylenes) containing tert-amine moieties.
Polymer, 49(12), 2808-2816 (2008)
Identification of chlorinated methoxybiphenyls as contaminants in fish and as potential interferences in the determination of chlorinated dibenzo-p-dioxins.
Analytical chemistry, 52(14), 2328-2332 (1980-12-01)
Bioorganic & medicinal chemistry, 17(17), 6463-6480 (2009-08-04)
The synthesis and structure-activity relationship analysis of a novel class of amide-based biaryl NR2B-selective NMDA receptor antagonists are presented. Some of the studied compounds are potent, selective, non-competitive, and voltage-independent antagonists of NR2B-containing NMDA receptors. Like the founding member of
The Journal of organic chemistry, 72(15), 5809-5812 (2007-06-26)
On-line monitoring of Stille reactions was performed via direct infusion electrospray ionization mass spectrometry (ESI-MS) and its tandem version (ESI-MS/MS). When operated in the positive ion mode, ESI(+)-MS was able to transfer, directly from solution to the gas phase, the
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