(2-Bromoethyl)benzene, 98%
(2-Bromoethyl)benzene, 98%
(2-Bromoethyl)benzene, 98%
(2-Bromoethyl)benzene, 98%
Thermo Scientific Chemicals

(2-Bromoethyl)benzene, 98%

CAS: 103-63-9 | C8H9Br | 185.064 g/mol
Have Questions?
變更視圖buttonViewtableView
Quantity:
100 g
500 g
產品號碼 A12528.36
亦稱為 A12528-36
價格 (TWD)
-
申請報價
Quantity:
500 g
Request bulk or custom format
化學識別
CAS103-63-9
IUPAC Name(2-bromoethyl)benzene
Molecular FormulaC8H9Br
InChI KeyWMPPDTMATNBGJN-UHFFFAOYSA-N
SMILESBrCCC1=CC=CC=C1
檢視更多
規格Specification Sheet規格表
Appearance (Color)Clear, colourless to pale yellow
Formliquid
Assay (GC)> 97.5%
Refractive Index1.5550 - 1.5580 @20?C
(2-Bromoethyl)benzene is used in the preparation of phenelzine by reacting with hydrazine. It is also used as a starting material to prepare various beta-phenethyl derivatives, active pharmaceutical ingredients, and fragrances. It finds application as a flame retardant.

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-Bromoethyl)benzene is used in the preparation of phenelzine by reacting with hydrazine. It is also used as a starting material to prepare various beta-phenethyl derivatives, active pharmaceutical ingredients, and fragrances. It finds application as a flame retardant.

Solubility
Miscible with ether and benzene. Immiscible with water.

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

General References:

  1. Shukla, P.; Sharma, A.; Pallavi, B.; Cheng, C. H. Nickel-catalyzed reductive Heck type coupling of saturated alkyl halides with acrylates and oxabenzonorbornadiene. Tetrahedron 2015, 71 (15), 2260-2266.
  2. Huang, Y. B.; Yan, L.; Chen, M. Y.; Guo, Q. X.; Fu, Y. Selective hydrogenolysis of phenols and phenyl ethers to arenes through direct C-O cleavage over ruthenium-tungsten bifunctional catalysts. Green Chem. 2015, 17 (5), 3010-3017.