3-Bromobenzonitrile, 99%
3-Bromobenzonitrile, 99%
3-Bromobenzonitrile, 99%
3-Bromobenzonitrile, 99%
Thermo Scientific Chemicals

3-Bromobenzonitrile, 99%

CAS: 6952-59-6 | C7H4BrN | 182.02 g/mol
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Catalog number A13317.09
also known as A13317-09
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Chemical Identifiers
CAS6952-59-6
IUPAC Name3-bromobenzonitrile
Molecular FormulaC7H4BrN
InChI KeySTXAVEHFKAXGOX-UHFFFAOYSA-N
SMILESBrC1=CC=CC(=C1)C#N
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to pale yellow
FormCrystals, crystalline powder or fused solid
Assay (GC)≥98.5%
Identification (FTIR)Conforms
3-Bromobenzonitrile is involved in the Suzuki reaction under solvent-free conditions.

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
3-Bromobenzonitrile is involved in the Suzuki reaction under solvent-free conditions.

Solubility
Soluble in water (0.2 g/L)

Notes
Store at room temperature. Incompatible with oxidizing agents. Ensure adequate ventilation.
RUO – Research Use Only

General References:

  1. Wenbin Lin .; Owen R. Evans.; Ren-Gen Xiong.; Zhiyong Wang. Supramolecular Engineering of Chiral and Acentric 2D Networks. Synthesis, Structures, and Second-Order Nonlinear Optical Properties of Bis(nicotinato)zinc and Bis{3-[2-(4-pyridyl)ethenyl]benzoato}cadmium.J. Am. Chem. Soc. 1998, 120 (50),13272-13273 .
  2. D. E. Pearson.; W. E. Stamper.; B. R. Suthers. The Swamping Catalyst Effect. V. The Halogenation of Aromatic Acid Derivatives. J. Org. Chem. 1963, 28 (11),3147-3149 .