• 图片1

2-Bromostyrene

  • CasNo:2039-88-5

Product Description

Factory Export Top Purity 2-Bromostyrene 2039-88-5 In Stock

  • Molecular Formula: C8H7Br
  • Molecular Weight: 183.048
  • Appearance/Colour: Clear colorless liquid 
  • Melting Point: 7 °C 
  • Refractive Index: n20/D 1.592(lit.)  
  • Boiling Point: 209.883 °C at 760 mmHg 
  • Flash Point: 83.932 °C 
  • PSA： 0.00000 
  • Density: 1.391 g/cm3 
  • LogP: 3.09210 

2-Bromostyrene(Cas 2039-88-5) Usage

InChI:InChI=1/C8H7Br/c1-2-7-5-3-4-6-8(7)9/h2-6H,1H2

2039-88-5 Relevant articles

-

Marvel,Moon

, p. 45,48 (1940)

-

Radical-Mediated 1,2-Formyl/Carbonyl Functionalization of Alkenes and Application to the Construction of Medium-Sized Rings

Li, Zhong-Liang,Li, Xiao-Hua,Wang, Na,Yang, Ning-Yuan,Liu, Xin-Yuan

, p. 15100 - 15104 (2016)

A novel radical 1,2-formylfunctionalizat...

The photoredox-catalyzed hydrosulfamoylation of styrenes and its application in the novel synthesis of naratriptan

Chen, Miaomiao,Ding, Xin,Gao, Yongyue,He, Xingxing,Kang, Jin,Lu, Aidang,Wang, Qingmin,Wang, Ziwen,Zhang, Mingjun

supporting information, p. 9140 - 9143 (2021/09/14)

The hydrosulfamoylation of diverse aryl ...

A Transient Directing Group Strategy Enables Enantioselective Multicomponent Organofluorine Synthesis

Engle, Keary M.,Gao, Yang,Li, Zi-Qi,Liu, Mingyu,Liu, Zhonglin,Oxtoby, Lucas J.,Tran, Van T.

supporting information, p. 8962 - 8969 (2021/07/01)

The vicinal fluorofunctionalization of a...

Sequential Addition of Amines to Nitrile and Carbon-Carbon Multiple Bond: A Route to 7-Amino-5 H-dibenzo[ c,e]azepines

Hu, Kun,Liu, Ruiting,Zhou, Xigeng

supporting information, p. 6946 - 6950 (2021/09/11)

A rare earth metal-catalyzed sequential ...

Electrochemistry enabled selective vicinal fluorosulfenylation and fluorosulfoxidation of alkenes

Jiang, Yimin,Shi, Zhaojiang,Wu, Jinnan,Wu, Shaofen,Ye, Keyin,Yu, Yi,Yuan, Yaofeng

supporting information, (2021/11/17)

Both sulfur and fluorine play important ...

2039-88-5 Process route

2-(2'bromophenyl)-1-iodoethane
113163-19-2

2-(2'bromophenyl)-1-iodoethane

1-bromo-2-(2-bromoethyl)benzene
1074-15-3

1-bromo-2-(2-bromoethyl)benzene

ethylbenzene
100-41-4,27536-89-6

ethylbenzene

1-bromo-2-ethylbenzene
1973-22-4

1-bromo-2-ethylbenzene

2-phenethyl iodide
17376-04-4

2-phenethyl iodide

2-bromostyrene
2039-88-5

2-bromostyrene

1-phenyl-2-bromoethane
103-63-9

1-phenyl-2-bromoethane

Conditions
Conditions Yield
With methanol; tert.-butyl lithium; In tetrahydrofuran; at -98 ℃; Product distribution; Mechanism;
2-[3-(2-bromophenyl)-1-phenylpropyl]-4,4-dimethyl-2-oxazoline
868069-27-6

2-[3-(2-bromophenyl)-1-phenylpropyl]-4,4-dimethyl-2-oxazoline

4,4-dimethyl-2-(1'-phenylindan-1'-yl)-2-oxazoline

4,4-dimethyl-2-(1'-phenylindan-1'-yl)-2-oxazoline

styrene
100-42-5,25038-60-2,25247-68-1,28213-80-1,28325-75-9,79637-11-9,9003-53-6

styrene

2-bromostyrene
2039-88-5

2-bromostyrene

Conditions
Conditions Yield
With lithium diisopropyl amide; In tetrahydrofuran; at 20 ℃; for 48h;
75%
With lithium diisopropyl amide; In tetrahydrofuran; at 20 ℃; for 20h;
50 % Spectr.

2039-88-5 Upstream products

  • 7345-79-1
    7345-79-1

    2-bromocinnamic acid

  • 127-08-2
    127-08-2

    potassium acetate

  • 102921-26-6
    102921-26-6

    (1,2-dibromoethyl)benzene

  • 563-63-3
    563-63-3

    silver(I) acetate

2039-88-5 Downstream products

  • 1973-22-4
    1973-22-4

    1-bromo-2-ethylbenzene

  • 28272-96-0
    28272-96-0

    2-vinylbenzaldehyde

  • 155504-10-2
    155504-10-2

    trans-1-(2-bromophenyl)-2-(3-bromophenyl)ethene

  • 78926-48-4
    78926-48-4

    o-(formyl-D1 )styrene

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