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Allyl acetate information


Allyl acetate
Skeletal formula of allyl acetate
Ball-and-stick model of the allyl acetate molecule
Names
Preferred IUPAC name
Prop-2-enyl acetate[1]
Other names
2-Propenyl acetate
Allyl acetate
Identifiers
CAS Number
  • 591-87-7 checkY
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL1890774
ChemSpider
  • 13862665 ☒N
ECHA InfoCard 100.008.851 Edit this at Wikidata
EC Number
  • 209-734-8
PubChem CID
  • 11584
RTECS number
  • AF1750000
UNII
  • E4U5E5990I
UN number 2333
CompTox Dashboard (EPA)
  • DTXSID9024437 Edit this at Wikidata
InChI
  • InChI=1S/C5H8O2/c1-3-4-7-5(2)6/h3H,1,4H2,2H3 ☒N
    Key: FWZUNOYOVVKUNF-UHFFFAOYSA-N ☒N
SMILES
  • C=CCOC(C)=O
Properties
Chemical formula
C5H8O2
Molar mass 100.117 g·mol−1
Appearance Colorless liquid
Density 0.928 g/cm3
Boiling point 103 °C (217 °F; 376 K)
Solubility in water
slightly soluble
Magnetic susceptibility (χ)
-56.7·10−6 cm3/mol
Hazards
GHS labelling:
Pictograms
GHS02: FlammableGHS06: ToxicGHS07: Exclamation mark
Signal word
Danger
Hazard statements
H225, H301, H312, H319, H330
Precautionary statements
P210, P233, P240, P241, P242, P243, P260, P264, P270, P271, P280, P284, P301+P310, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P320, P321, P322, P330, P337+P313, P363, P370+P378, P403+P233, P403+P235, P405, P501
Autoignition
temperature
374 °C (705 °F; 647 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Allyl acetate is an organic compound with formula C3H5OC(O)CH3. This colourless liquid is a precursor to especially allyl alcohol, which is a useful industrial intermediate. It is the acetate ester of allyl alcohol.

  1. ^ "Allyl acetate".

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Allyl acetate

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Allyl acetate is an organic compound with formula C3H5OC(O)CH3. This colourless liquid is a precursor to especially allyl alcohol, which is a useful industrial...

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C5H8O2

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Carbonyl allylation

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rely on preformed allylmetal reagents, the Krische allylation exploits allyl acetate for enantioselective carbonyl allylation. Selected methods for asymmetric...

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