| Company Name: |
Alfa Aesar |
| Tel: |
400-6106006 |
| Email: |
saleschina@alfa-asia.com |
| Company Name: |
Sigma-Aldrich |
| Tel: |
021-61415566 800-8193336 |
| Email: |
orderCN@merckgroup.com |
|
| | Phenethylzinc bromide Basic information |
| | Phenethylzinc bromide Chemical Properties |
| Boiling point | 65 °C | | density | 0.965 g/mL at 25 °C | | Fp | 1 °F | | storage temp. | 2-8°C | | Water Solubility | Reacts with water. | | Sensitive | Air Sensitive | | InChI | 1S/C8H9.BrH.Zn/c1-2-8-6-4-3-5-7-8;;/h3-7H,1-2H2;1H;/q;;+1/p-1 | | InChIKey | SEXSOTWHLBYVNF-UHFFFAOYSA-M | | SMILES | Br[Zn]CCc1ccccc1 | | CAS DataBase Reference | 308796-14-7 |
| Hazard Codes | F,Xn | | Risk Statements | 14-19-22-36/38-40-36/37-11 | | Safety Statements | 16-26-33-36-36/37 | | RIDADR | UN 2056 3/PG 2 | | WGK Germany | 1 | | HazardClass | 4.3 | | Storage Class | 3 - Flammable liquids | | Hazard Classifications | Carc. 2 Eye Irrit. 2 Flam. Liq. 2 STOT SE 3 |
| | Phenethylzinc bromide Usage And Synthesis |
| Uses | Phenethylzinc bromide can be used as a reagent:
- In the transition metal-catalyzed Negishi cross-coupling reaction to prepare aryl or heteroaryl derivatives by reacting with organic halides or triflates via carbon-carbon bond formation.
- To prepare (4-phenyl-1-butyn-1-yl)benzene by reacting with phenylacetylene via palladium-catalyzed cross-coupling reaction.
- To synthesize benzyl substituted thienopyrimidine derivatives.
|
| | Phenethylzinc bromide Preparation Products And Raw materials |
|