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523062

Sigma-Aldrich

3-Vinylbenzaldehyde

97%

Sinónimos:

3-Ethenylbenzaldehyde, 3-Formylstyrene, m-Formylstyrene, m-Vinylbenzaldehyde

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About This Item

Fórmula lineal:
H2C=CHC6H4CHO
Número de CAS:
19955-99-8
Peso molecular:
132.16
MDL number:
MFCD02093761
UNSPSC Code:
12352100
PubChem Substance ID:
24874294
NACRES:
NA.22

Quality Level

100

assay

97%

refractive index

n20/D 1.58 (lit.)

density

1.04 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

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

InChI

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

InChI key

CATOVPRCMWIZLR-UHFFFAOYSA-N

General description

3-Vinylbenzaldehyde (3-VBAL) contains a vinyl group bonded to the aromatic ring of benzaldehyde. Pulsed plasma polymerization of 3-VBAL has been described.

Application

3-Vinylbenzaldehyde may be used in the preparation of:
  • 2-(3-vinylphenyl)-1,3-dioxolane
  • various substituted imines
  • monomer bearing a 2,4,5-triphenylimidazole moiety
  • poly(3-vinylbenzaldehyde-co-dimethylacrylamide) (PVBA-co-PDMA) copolymers

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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)
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
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
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)
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