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523062

Sigma-Aldrich

3-Vinylbenzaldehyde

97%

Synonym(s):

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

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$332.00

About This Item

Linear Formula:
H2C=CHC6H4CHO
CAS Number:
19955-99-8
Molecular Weight:
132.16
MDL number:
MFCD02093761
UNSPSC Code:
12352100
PubChem Substance ID:
24874294
NACRES:
NA.22
assay:
97%

$332.00

In StockDetails

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Quality Level

100

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

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.[1] Pulsed plasma polymerization of 3-VBAL has been described.[2]

application

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

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ0302
MKCR7934
MKCK6982
MKCG2668
MKCD1872

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New benzylidene oxazolone derived polymeric photoswitches for light-induced tunable thermoresponsive behaviors.
Balamurugan A and Lee H.
Polym. Chem., 5(22), 6426-6430 (2014)
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
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
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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