(1-Bromoethyl)benzene

95%

Reagent Code: #113013
label
Alias (1-bromoethyl)benzene; a-bromoethylbenzene, 1-phenylethyl bromide, 1-bromoethylbenzene
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CAS Number 585-71-7

science Other reagents with same CAS 585-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.06 g/mol
Formula C₈H₉Br
badge Registry Numbers
EC Number 209-560-2
MDL Number MFCD00000139
thermostat Physical Properties
Melting Point -65°C
Boiling Point 94 °C16 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.356 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is often employed in alkylation reactions, where it introduces the 1-phenylethyl group into target molecules, enhancing their structural complexity. Additionally, it finds application in the development of specialty chemicals, including dyes and fragrances, due to its ability to modify aromatic compounds. Its reactivity with nucleophiles makes it valuable in creating carbon-carbon bonds, essential in constructing complex organic frameworks.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 95-100%
Refractive Index (20 °C) 1.559-1.562
Specific Gravity (20/20 Degrees Celsius) 1.35-1.362
Appearance Colorless to light yellow liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿710.00
inventory 25g
10-20 days ฿2,800.00

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(1-Bromoethyl)benzene
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is often employed in alkylation reactions, where it introduces the 1-phenylethyl group into target molecules, enhancing their structural complexity. Additionally, it finds application in the development of specialty chemicals, including dyes and fragrances, due to its ability to modify aromatic compounds. Its reactivity with nucleophiles makes it valuable in c

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. It is often employed in alkylation reactions, where it introduces the 1-phenylethyl group into target molecules, enhancing their structural complexity. Additionally, it finds application in the development of specialty chemicals, including dyes and fragrances, due to its ability to modify aromatic compounds. Its reactivity with nucleophiles makes it valuable in creating carbon-carbon bonds, essential in constructing complex organic frameworks.

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