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2,6-Dichlorostyrene, 96%, stab. with 0.1% 4-tert-butylcatechol
2,6-Dichlorostyrene, 96%, stab. with 0.1% 4-tert-butylcatechol
2,6-Dichlorostyrene, 96%, stab. with 0.1% 4-tert-butylcatechol
Thermo Scientific Chemicals

2,6-Dichlorostyrene, 96%, stab. with 0.1% 4-tert-butylcatechol

CAS: 28469-92-3 | C8H6Cl2 | 173.04 g/mol
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Catalog number L07860.06
also known as L07860-06
Price (USD)
80.65
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Online exclusive
Ends: 30-Jun-2026
95.20
Save 14.55 (15%)
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Quantity:
5 g
Request bulk or custom format
Price (USD)
80.65
Special offer
Online exclusive
Ends: 30-Jun-2026
95.20
Save 14.55 (15%)
Each
Chemical Identifiers
CAS28469-92-3
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow
Refractive Index1.5710-1.5770 @ 20?C
Solution Test(10% w/v in Methanol): Clear
Assay (GC)≥95.0%
Identification (FTIR)Conforms
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2,6-Dichlorostyrene is used in the preparation of 1,3-dichloro-2-(1,2-dibromo-ethyl)-benzene by bromination reaction using bromine.

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
2,6-Dichlorostyrene is used in the preparation of 1,3-dichloro-2-(1,2-dibromo-ethyl)-benzene by bromination reaction using bromine.

Solubility
Immiscible with water.

Notes
Store in a cool place. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Wang, B.; Lee, Y. M.; Seo, M. S.; Nam, W. Mononuclear Nonheme Iron(III)-Iodosylarene and High-Valent Iron-Oxo Complexes in Olefin Epoxidation Reactions. Angew. Chem. Int. Ed. 2015, 54 (40), 11740-11744.
  2. Wang, F.; Wang, D.; Mu, X.; Chen, P.; Liu, G. Copper-Catalyzed Intermolecular Trifluoromethylarylation of Alkenes: Mutual Activation of Arylboronic Acid and CF3+ Reagent. J. Am. Chem. Soc. 2014, 136 (29), 10202-10205.