4-Cyanostyrene, 97%, stab. with 0.05% 4-tert-butyl catechol
4-Cyanostyrene, 97%, stab. with 0.05% 4-tert-butyl catechol
4-Cyanostyrene, 97%, stab. with 0.05% 4-tert-butyl catechol
4-Cyanostyrene, 97%, stab. with 0.05% 4-tert-butyl catechol
Thermo Scientific Chemicals

4-Cyanostyrene, 97%, stab. with 0.05% 4-tert-butyl catechol

CAS: 3435-51-6 | C9H7N | 129.16 g/mol
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25 g
Catalog number B24395.14
also known as B24395-14
Price (EUR)
870,00
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Quantity:
25 g
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Price (EUR)
870,00
Each
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Chemical Identifiers
CAS3435-51-6
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear, colorless
Assay (GC)>96.0%
Solution Test(10% v/v in Methanol) : Clear
Refractive Index1.5750-1.5800 @ 20?C
Solution Test(10% v/v in Diethyl ether) : Clear
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4-Cyanostyrene is used as an intermediate in organic synthesis. It is used in the preparation of poly(4-cyanostyrene) polymer , which is a macromolecular device having nanoscale order and finds a wide range of potential applications.

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
4-Cyanostyrene is used as an intermediate in organic synthesis. It is used in the preparation of poly(4-cyanostyrene) polymer , which is a macromolecular device having nanoscale order and finds a wide range of potential applications.

Solubility
Immiscible with water.

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

General References:

  1. Wei, W.; Liu, X.; Yang, D.; Dong, R.; Cui, Y.; Yuan, F.; Wang, H. Direct difunctionalization of alkenes with sulfinic acids and NBS leading to β-bromo sulfones. Tetrahedron Lett. 2015, 56 (14), 1808-1811.
  2. Tang, S.; Liu, K.; Long, Y.; Gao, X.; Gao, M.; Lei, A. Iodine-Catalyzed Radical Oxidative Annulation for the Construction of Dihydrofurans and Indolizines. Org. Lett. 2015, 17 (10), 2404-2407.