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3-VINYLBENZALDEHYDE

Names

[ CAS No. ]:
19955-99-8

[ Name ]:
3-VINYLBENZALDEHYDE

[Synonym ]:
3-vinylbenzaldhyde
m-ethenylbenzaldehyde
Benzaldehyde,3-ethenyl
MFCD02093761
3-vinyl benzaldehyde
m-vinylbenzaldehyde

Chemical & Physical Properties

[ Density]:
1.04 g/mL at 25ºC(lit.)

[ Boiling Point ]:
230.2ºC at 760 mmHg

[ Molecular Formula ]:
C9H8O

[ Molecular Weight ]:
132.15900

[ Flash Point ]:
210 °F

[ Exact Mass ]:
132.05800

[ PSA ]:
17.07000

[ LogP ]:
2.14210

[ Vapour Pressure ]:
0.0668mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.58(lit.)

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2912299000

Customs

[ HS Code ]: 2912299000

[ Summary ]:
2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Chemoselective synthesis of substituted imines, secondary amines, and beta-amino carbonyl compounds from nitroaromatics through cascade reactions on gold catalysts.

Chemistry 15(33) , 8196-203, (2009)

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 go...

Mimicking a Stenocara beetle's back for microcondensation using plasmachemical patterned superhydrophobic-superhydrophilic surfaces.

Langmuir 23(2) , 689-93, (2007)

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 depositi...

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)


More Articles


Related Compounds