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Merck
CN

523062

3-乙烯基苯甲醛

97%

别名:

3-乙烯基苯甲醛, 3-甲酰苯乙烯, 间乙烯基苯甲醛, 间甲酰苯乙烯

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关于此项目

线性分子式:
H2C=CHC6H4CHO
化学文摘社编号:
分子量:
132.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
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产品名称

3-乙烯基苯甲醛, 97%

InChI

1S/C9H8O/c1-2-8-4-3-5-9(6-8)7-10/h2-7H,1H2

SMILES string

[H]C(=O)c1cccc(C=C)c1

InChI key

CATOVPRCMWIZLR-UHFFFAOYSA-N

assay

97%

refractive index

n20/D 1.58 (lit.)

density

1.04 g/mL at 25 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

Quality Level

Application

3-乙烯基苯甲醛可用于制备:
  • 2-(3-乙烯基苯基)-1,3-二氧戊环
  • 各种取代亚胺
  • 含 2,4,5-三苯基咪唑基团的单体
  • 聚(3-乙烯基苯甲醛-co-二甲基丙烯酰胺(PVBA- co-PDMA)共聚物

General description

3-乙烯基苯甲醛 (3-VBAL) 含有与苯甲醛芳香环结合的乙烯基。本文描述了 3-VBAL 的脉冲等离子体聚合。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

210.0 °F - closed cup

flash_point_c

98.9 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Protection and polymerization of functional monomers. 15. Anionic living polymerizations of 2-(3-vinylphenyl)-1, 3-dioxolane and related monomers.
Ishizone T, et al.
Macromolecules, 24(7), 1449-1454 (1991)
New benzylidene oxazolone derived polymeric photoswitches for light-induced tunable thermoresponsive behaviors.
Balamurugan A and Lee H.
Polym. Chem., 5(22), 6426-6430 (2014)
A novel de-cross-linking system from cross-linked polymer to linear polymer utilizing pressure or visible light irradiation.
Iwamura T and Sakaguchi M.
Macromolecules, 41(23), 8995-8999 (2008)
R P Garrod et al.
Langmuir : the ACS journal of surfaces and colloids, 23(2), 689-693 (2007-01-11)
A simple two-step plasmachemical methodology is outlined for the fabrication of microcondensor surfaces. This comprises the creation of a superhydrophobic background followed by pulsed plasma deposition of a hydrophilic polymer array. Microcondensation efficiency has been explored in terms of the
Laura L Santos et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(33), 8196-8203 (2009-07-18)
Substituted imines, alpha,beta-unsaturated imines, substituted secondary amines, and beta-amino carbonyl compounds have been synthesized by means of new cascade reactions with mono- or bifunctional gold-based solid catalysts under mild reaction conditions. The related synthetic route involves the hydrogenation of a

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