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1-Bromo-2-iodobenzene, 98+%, stab. with copper, Thermo Scientific Chemicals
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Catalog number A17020.06
also known as A17020-06
Price (USD)/ Each
47.10
-
Quantity:
5 g
Price (USD)/ Each
47.10
1-Bromo-2-iodobenzene, 98+%, stab. with copper, Thermo Scientific Chemicals
Catalog numberA17020.06
Price (USD)/ Each
47.10
-
Chemical Identifiers
CAS583-55-1
IUPAC Name1-bromo-2-iodobenzene
Molecular FormulaC6H4BrI
InChI KeyOIRHKGBNGGSCGS-UHFFFAOYSA-N
SMILESBrC1=CC=CC=C1I
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to yellow to brown
Identification (FTIR)Conforms
Refractive Index1.6625-1.6675 @ 20?C
FormLiquid
Assay (GC)≥98.0%
2-Bromoiodobenzene is used in the synthesis of diarylamines.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Bromoiodobenzene is used in the synthesis of diarylamines.
Solubility
Not miscible or difficult to mix in water.
Notes
Light Sensitive. Protect from light. Store away from oxidizing agents.
2-Bromoiodobenzene is used in the synthesis of diarylamines.
Solubility
Not miscible or difficult to mix in water.
Notes
Light Sensitive. Protect from light. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- María E Budén.; Victoria A Vaillard.; Sandra E Martin.; Roberto A Rossi. Synthesis of carbazoles by intramolecular arylation of diarylamide anions.J Org Chem.2009,74(12), 4490-4498.
- Biao Lu.; Bao Wang.; Yihua Zhang.; and Dawei Ma. CuI-Catalyzed Domino Process to 2,3-Disubstituted Benzofurans from 1-Bromo-2-Iodobenzenes and β-Keto Esters.J. Org. Chem.,2007,72,(14), 5337-5341.
- Benzyne precursor. In the presence of excess of a Grignard reagent, the initially formed benzyne undergoes nucleophilic addition to give an ortho-substituted phenylmagnesium halide: Synth. Commun., 18, 1749 (1988).
- Regioselective Suzuki coupling with arylboronic acids has been achieved giving 2-bromobiphenyl derivatives: Synlett, 207 (1992).