Allylbenzene
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Preferred IUPAC name (Prop-2-enyl)benzene[1] | |
Other names 3-Phenyl-1-propene; 2-Propenylbenzene | |
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ECHA InfoCard | 100.005.542 |
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Properties | |
Chemical formula | C9H10 |
Molar mass | 118.179 g·mol−1 |
Appearance | Colorless liquid |
Density | 0.893 g/cm3 |
Melting point | −40 °C (−40 °F; 233 K) |
Boiling point | 156 °C (313 °F; 429 K) |
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Occupational safety and health (OHS/OSH): | |
Main hazards | Flammable liquid and vapor, May be fatal if swallowed and enters airways |
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Pictograms | [2] |
Danger | |
Hazard statements | H226, H304[2] |
Precautionary statements | P210, P233, P240, P241, P242, P243, P280, P301+P316, P303+P361+P353, P331, P370+P378, P403+P235, P405, P501[2] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references |
Chemical compound
Allylbenzene or 3-phenylpropene is an organic compound with the formula C6H5CH2CH=CH2. It is a colorless liquid. The compound consists of a phenyl group attached to an allyl group. Allylbenzene isomerizes to trans-propenylbenzene.[3]
In plant biochemistry, the allylbenzene skeleton is the parent (simplest representation) of many phenylpropanoids. Prominent allylbenzenes include eugenol, safrole, and many others.[4]
References
- ^ "Allylbenzene".
- ^ a b c "Allylbenzene".
- ^ Hassam, Mohammad; Taher, Abu; Arnott, Gareth E.; Green, Ivan R.; van Otterlo, Willem A. L. (2015). "Isomerization of Allylbenzenes". Chemical Reviews. 115 (11): 5462–5569. doi:10.1021/acs.chemrev.5b00052. PMID 25993416.
- ^ Vogt, Thomas (2010). "Phenylpropanoid Biosynthesis". Molecular Plant. 3 (1): 2–20. doi:10.1093/mp/ssp106. PMID 20035037.
External links
- Media related to Allylbenzene at Wikimedia Commons