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Assay
97%
form
solid
mp
124-128 °C (lit.)
SMILES string
Ic1ccc(cc1)C#N
InChI
1S/C7H4IN/c8-7-3-1-6(5-9)2-4-7/h1-4H
InChI key
XOKDXPVXJWTSRM-UHFFFAOYSA-N
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Application
4-Iodobenzonitrile may be used in the synthesis of the following:
- ethyl-4′-cyano-4-nitro[1,1′-biphenyl]-2-carboxylate via a multi-step reaction process
- 2-(4-cyanophenyl)tellurophene obtained via Stille coupling with tellurophene
- 2,5-bis(4-cyanophenyl)tellurophene obtained via Stille coupling with 2,5-bis(trimethylstannyl)tellurophene
- ethyl-4′-cyano-6-{[(E)-phenylmethylidene]amino}[1,1′-biphenyl]-3-carboxylate via a multi-step reaction process
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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Find documentation for the products that you have recently purchased in the Document Library.
Molecules (Basel, Switzerland), 24(10) (2019-05-30)
The crystal structure of 4-iodobenzonitrile, which is monoclinic (space group I2/a) under ambient conditions, contains chains of molecules linked through C≡N···I halogen-bonds. The chains interact through CH···I, CH···N and π-stacking contacts. The crystal structure remains in the same phase up
"Preparation and reactions of functionalized arylmagnesium reagents"
Synthesis, 2002(04), 0565-0569 (2002)
"Synthesis of Nitro-Substituted Polyfunctional Biphenyls by Negishi Cross-Coupling of o-Nitroarylzinc Reagents"
Advanced Synthesis & Catalysis, 346(07), 709-712 (2004)
"Synthesis and stille cross-coupling reactions of 2-(tributylstannyl)-and 2, 5-bis (trimethylstannyl) tellurophene"
Synthesis, 2009(19), 3214-3218 (2009)
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