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Merck
CN

124141

4-溴苯乙烯

contains 0.05% 3,5-di-tert-butylcatechol as inhibitor, 97%

别名:

1-(4-溴苯基)乙烯, 1-溴-4-乙烯基苯, 1-溴-4-乙烯苯, 4-乙烯基-1-溴苯, 溴苯乙烯

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关于此项目

线性分子式:
H2C=CHC6H4Br
化学文摘社编号:
分子量:
183.05
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
218-022-6
Beilstein/REAXYS Number:
1634204
MDL number:
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InChI key

WGGLDBIZIQMEGH-UHFFFAOYSA-N

InChI

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

SMILES string

Brc1ccc(C=C)cc1

assay

97%

form

liquid

contains

0.05% 3,5-di-tert-butylcatechol as inhibitor

refractive index

n20/D 1.594 (lit.)

bp

89 °C/16 mmHg (lit.)

density

1.4 g/mL at 25 °C (lit.)

storage temp.

−20°C

Quality Level

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Application

4-溴苯乙烯已用于以下研究:
  • 苯乙烯乙烯基的化学和生化特性的结构活性相关性 (SAR) 研究。
  • 合成具有4-代苯乙烯基取代基的倍半硅氧烷(SQ)。
  • 调查光Br端自组装单层(SAMs) 在二氧化硅(111)上的光化学生长。
  • 通过Heck反应合成聚(1,4-亚苯基亚乙烯基)。
  • 通过烯烃交叉复分解合成硝基烯烃。

General description

4-溴苯乙烯是卤代苯乙烯衍生物。只有当最低频率的扭转运动发生在大约80cm-1处时,4-溴苯乙烯的质子谱才显示出与平面基态结构一致的偶极耦合。在乙酸钠和Hermann催化剂存在的情况下,其可在N,N-二甲基乙酰胺中与2-溴-6-甲氧基萘进行Heck反应,得到二芳基乙烯。

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

167.0 °F - closed cup

flash_point_c

75 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

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Synthesis and characterization of new hexahelicene derivatives.
Aloui F, et al.
Tetrahedron Letters, 48(11), 2017-2020 (2007)
Graham P Marsh et al.
Organic letters, 9(14), 2613-2616 (2007-06-07)
A synthesis of highly functionalized nitroalkenes is reported that utilizes a cross metathesis (CM) reaction between simple aliphatic nitro compounds and a range of substituted alkenes. This chemistry offers a simple and attractive route to nitroalkenes that would otherwise be
Synthesis of monomers and polymers by the Heck reaction.
Heitz W, et al.
Makromol. Chem., 189(1), 119-127 (1988)
Structural characterization of 4-bromostyrene self-assembled monolayers on Si (111).
Basu R, et al.
Langmuir, 23(4), 1905-1911 (2007)
Małgorzata Bołt et al.
Materials (Basel, Switzerland), 13(18) (2020-09-12)
Bifunctional silsesquioxanes create an attractive group of compounds with a wide range of potential applications, and recently they have gained much interest. They are known to be obtained mainly via hydrosilylation, but we disclose novel synthetic protocols based on different

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