2-Bromonaphthalene, 98+%, Thermo Scientific Chemicals
2-Bromonaphthalene, 98+%, Thermo Scientific Chemicals
2-Bromonaphthalene, 98+%, Thermo Scientific Chemicals
2-Bromonaphthalene, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Bromonaphthalene, 98+%, Thermo Scientific Chemicals

CAS: 580-13-2 | C10H7Br | 207.07 g/mol
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Quantity:
25 g
5 g
Catalog number ALFA15300.14
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Quantity:
25 g
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Chemical Identifiers
CAS3240-34-4
IUPAC Name(acetyloxy)(phenyl)-λ³-iodanyl acetate
Molecular FormulaC10H11IO4
InChI KeyZBIKORITPGTTGI-UHFFFAOYSA-N
SMILESCC(=O)O[I](OC(C)=O)C1=CC=CC=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to light yellow
Appearance (Form)Crystalline powder
Infrared spectrumConforms
Titration Iodometric>=97.5 %
Melting point159°C to 164°C
2-Bromonaphthalene is used as a raw material in the preparation of biaryls through Suzuki cross coupling reaction. Further, it plays a vital role in the preparation of dyes. It is also used to study potential tumorigenicity.

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-Bromonaphthalene is used as a raw material in the preparation of biaryls through Suzuki cross coupling reaction. Further, it plays a vital role in the preparation of dyes. It is also used to study potential tumorigenicity.

Solubility
Slightly soluble in water.

Notes
Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. The Grignard reagent has been reacted with N-benzylproline methyl ester in the synthesis of oxazaborolidines (compare (S)-2-Methyl-CBS-oxazaborolidine monohydrate, L09219) for use as chiral auxiliaries: J. Org. Chem., 56, 442 (1991).
  2. Hopkins, B. A.; Garlets, Z. J.; Wolfe, J. P. Development of Enantioselective Palladium-Catalyzed Alkene Carboalkoxylation Reactions for the Synthesis of Tetrahydrofurans. Angew. Chem. Int. Ed. 2015, 54 (45), 13390-13392
  3. Xu, L.; Suo, H.; Liang, X.; Wang, L.; Guo, Y.; Jiang, S. Au nanoparticle decorated graphene oxide as a novel coating for solid-phase microextraction. RSC Adv. 2015, 5 (52), 41536-41543.