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1,3-Dibromobenzene, 97+%, Thermo Scientific Chemicals
Catalog number: A12723.36
500 g, Each
Thermo Scientific Chemicals
1,3-Dibromobenzene, 97+%, Thermo Scientific Chemicals
Catalog number: A12723.36
500 g, Each
Quantity
Catalog number: A12723.36
also known as A12723-36
Price (USD)
Price: 974.00
Online price: 842.65
Your price:
Quantity
-
Chemical Identifiers
CAS
108-36-1
IUPAC Name
1,3-dibromobenzene
Molecular Formula
C6H4Br2
InChI Key
JSRLURSZEMLAFO-UHFFFAOYSA-N
SMILES
BrC1=CC(Br)=CC=C1
Specifications
Specification SheetAppearance (Color)
Clear colorless to pale yellow
Assay (GC)
≥97.0%
Refractive Index
1.6055-1.6105 @ 20?C
Form
Liquid
Identification (FTIR)
Conforms
Description
1,3-Dibromobenzene is used in Suzuki coupling reaction for the preparation of [n]metacyclophanes. It is used to prepare 5-(3-bromo-phenyl)-2,4-di-tert-butoxy-pyrimidine using Pd(0) (PPh3)4 as a reagent. Further, it undergoes solid-supported potassium fluoride-aluminum oxide palladium-catalyzed polyarylation reaction with phenyl boronic acid to get conjugated polyaryls.
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
1,3-Dibromobenzene is used in Suzuki coupling reaction for the preparation of [n]metacyclophanes. It is used to prepare 5-(3-bromo-phenyl)-2,4-di-tert-butoxy-pyrimidine using Pd(0) (PPh3)4 as a reagent. Further, it undergoes solid-supported potassium fluoride-aluminum oxide palladium-catalyzed polyarylation reaction with phenyl boronic acid to get conjugated polyaryls.
Solubility
Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
1,3-Dibromobenzene is used in Suzuki coupling reaction for the preparation of [n]metacyclophanes. It is used to prepare 5-(3-bromo-phenyl)-2,4-di-tert-butoxy-pyrimidine using Pd(0) (PPh3)4 as a reagent. Further, it undergoes solid-supported potassium fluoride-aluminum oxide palladium-catalyzed polyarylation reaction with phenyl boronic acid to get conjugated polyaryls.
Solubility
Immiscible with water.
Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only
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