(2-Bromoethyl)benzene

98%

  • Product Code: 113131
  Alias:    (2-bromoethyl)benzene; β-bromophenylethane, bromoethylbenzene, β-bromoethylbenzene, 2-phenylbromoethane
  CAS:    103-63-9
Molecular Weight: 185.06 g./mol Molecular Formula: C₈H₉Br
EC Number: 203-130-8 MDL Number: MFCD00000240
Melting Point: -56 °C Boiling Point: 220-221 °C(lit.)
Density: 1.355 g/mL at 25 °C(lit.) Storage Condition: 2~8°C
Product Description: (2-Bromoethyl)benzene is primarily used as an intermediate in organic synthesis. It is commonly employed in the production of pharmaceuticals, where it serves as a building block for the synthesis of various active compounds. Additionally, it is utilized in the creation of agrochemicals, contributing to the development of pesticides and herbicides. The compound is also valuable in polymer chemistry, where it acts as a precursor for the modification of polymers and the synthesis of specialty materials. Its reactivity, particularly the bromine atom, makes it a versatile reagent in alkylation and coupling reactions, enabling the formation of complex organic molecules.
Product Specification:
Test Specification
Purity (GC) 98-100
Refractive Index N20/D 1.556-1.558
Appearance Colorless To Yellow Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
25.000 10-20 days £9.95
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100.000 10-20 days £13.34
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500.000 10-20 days £42.29
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(2-Bromoethyl)benzene
(2-Bromoethyl)benzene is primarily used as an intermediate in organic synthesis. It is commonly employed in the production of pharmaceuticals, where it serves as a building block for the synthesis of various active compounds. Additionally, it is utilized in the creation of agrochemicals, contributing to the development of pesticides and herbicides. The compound is also valuable in polymer chemistry, where it acts as a precursor for the modification of polymers and the synthesis of specialty materials. Its reactivity, particularly the bromine atom, makes it a versatile reagent in alkylation and coupling reactions, enabling the formation of complex organic molecules.
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