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2114-39-8

  • Product Name:2-Bromo-1-phenylpropane
  • Molecular Formula:C9H11 Br
  • Appearance:clear colorless to light brown liquid
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Product Details

Appearance:clear colorless to light brown liquid

Purity:99%

High Purity 2-Bromo-1-phenylpropane 2114-39-8 Good Supplier

2114-39-8 Name

Name

2-Bromo-1-phenylpropane

Synonym

Benzene,(2-bromopropyl)-;2-BROMO-1-PHENYLPROPANE;(2-BROMOPROPYL)BENZENE;1-PHENYL-2-BROMO PROPANE;α-Methylphenethyl bromide;rac-(R*)-1-Phenyl-2-bromopropane;2-Bromo-1-phenylpropane,97%;2-Bromo-1-phenylpropane,98%

 

 Chemical & Physical Properties

Melting point 

-10°C (estimate)

Boiling point

107-109 °C16 mm Hg(lit.)

Density

1.291 g/mL at 25 °C(lit.)

Molecular Formula

C9H11Br

Molecular Weight

199.08800

Flash Point

195 °F

PSA

3.01250

Exact Mass

198.00400

Vapour Pressure

0.113mmHg at 25°C

Index of Refraction

n20/D 1.545(lit.)

High Purity 2-Bromo-1-phenylpropane 2114-39-8 Usage

2-Bromo-1-phenylpropane is a useful research chemical which is a liquid that is used as an intermediate in the production of styrene. It is prepared by the reaction of ethylmagnesium bromide with arylacetylene.

Chemical Properties

clear colorless to light brown liquid

InChI:InChI=1/C9H11Br/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8H,7H2,1H3

2114-39-8 Relevant articles

A Detailed Conformational Analysis of 2'Bromo'l' phenylpropane by High Resolution Nuclear Magnetic Resonance spectroscopy and Molecular Orbital Calculations

Paul Hazendonk

MASTER OF SCIENCE August, 1995

2-Bromo-1-phenylpropane is expected to exhibit all the above complications. Assuming a linear dependence of tJ* on electronegativity, 6J* can be predicted for 2-bromo-1-phenylpropane by extrapolating between the values for toluene and benzylfluoride using the electronegativity of the -CHBTCH, group.

Visible Light-Mediated Conversion of Alcohols to Bromides by a Benzothiadiazole-Containing Organic Photocatalyst

Li, Run,Gehrig, Dominik W.,Ramanan, Charusheela,Blom, Paul W. M.,Kohl, Fabien F.,Wagner, Manfred,Landfester, Katharina,Zhang, Kai A. I.

, p. 3852 - 3859 (2019/07/15)

The search for metal-free, stable and high effective photocatalysts with sufficient photo-redox potentials remains a key challenge for organic chemists. Here, we present a benzothiadiazole-containing molecular organic photocatalyst with redox potentials of ?1.30 V and +1.64 V vs. SCE. Lastly, no photo-bleaching effect is observed, demonstrating the high stability and recyclable of the designed organic photocatalyst. (Figure presented.).

2114-39-8 Process route

(±)-1-phenylpropanyl-2-yl methansulfonate
61380-47-0

(±)-1-phenylpropanyl-2-yl methansulfonate

1-phenylpropene
637-50-3

1-phenylpropene

(2-bromopropyl)-benzene
2114-39-8

(2-bromopropyl)-benzene

Conditions
Conditions Yield
With 1-n-butyl-3-methylimidazolim bromide; at 90 ℃; for 1h; Concentration; Temperature; Time; Inert atmosphere; Green chemistry;
95%
34%
3-phenyl-2-propanol
698-87-3,14898-87-4

3-phenyl-2-propanol

1-phenylpropene
637-50-3

1-phenylpropene

(2-bromopropyl)-benzene
2114-39-8

(2-bromopropyl)-benzene

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: pyridine / 20 °C
2: 1-n-butyl-3-methylimidazolim bromide / 1 h / 90 °C / Inert atmosphere; Green chemistry
With pyridine; 1-n-butyl-3-methylimidazolim bromide;
 

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