(E)-3-phenyl-2-propenal


cinnamal; (E)-cinnamaldehyde; cinnamaldehyde; trans-cinnamaldehyde; cinnamic aldehyde; cinnamyl aldehyde; cinnamylaldehyde; β-phenylacrolein; (2E)-3-phenylacrylaldehyde; 3-phenylpropenal; trans-3-phenylpropenal; (2E)-3-phenyl-2-propenal; (2E)-3-phenylprop-2-enal; (E)-3-phenyl-2-propenal; 3-phenylprop-2-enal
Links:🌍 Wikipedia, 📏 NIST, ⚗️ ChemSynthesis, 📖 PubMed
MeSH:Antimutagenic Agents; Antineoplastic Agents; Food Additives; Protective Agents; Antimutagenic Agents; Antineoplastic Agents; Food Additives; Protective Agents
CAS:[104-55-2]
Formula:C9H8O; 132.16 g/mol
InChiKey:KJPRLNWUNMBNBZ-QPJJXVBHSA-N
SMILES:O=C/C=C/c1ccccc1
Molecular structure of (E)-3-phenyl-2-propenal
Use:extracts; flavors; perfumes; soap perfumes; synthetic apricot, banana, butterscotch, cacao, almond, cherry, date, grenadine, plum, raspberry, and strawberry essences
Density:1.050 g/mL
Molar volume:125.9 mL/mol
Refractive index:1.619
Molecular refractive power:44.20 mL/mol
Dielectric constant:16.90
Dipole moment:4.08 D
Melting point:-8 °C
Boiling point:252 °C
Antoine equation
P(Torr) vs T(°C)
Vapour pressure vs temperature
Log10 partition octanol / water:1.90
Immiscible with:
1,2,3-propanetriol,    1,3-propanediol,    ethanediol
Miscible with:
(+-)-3-chloro-1,2-propanediol,    (R,S)-2,3-butanediol,    1,2-diacetoxyethane,    1,2-propanediol,    1-heptadecanol,    1-tetradecanol,    2,6,8-trimethyl-4-nonanone,    2,6-dimethyl-4-heptanone,    2-(2-butoxyethoxy)ethanol,    2-(2-ethoxyethoxy)ethanol,    2-(2-methoxyethoxy)ethanol,    2-bromoethyl acetate,    2-butoxyethanol,    2-chloroethanol,    2-ethoxyethanol,    2-ethylbutanoic acid,    2-methoxyethanol,    2-phenoxyethanol,    2-propanone,    3,6,9-trioxaundecane,    3-chloropropanol,    3-heptanol,    3-methyl-2-butanone,    3-methylbutyl acetate,    4-methylpentanoic acid,    4-oxa-2,6-heptandiol,    N,N-diethylformamide,    N,N-dipropylaniline,    a-methylbenzyldimethylamine,    benzene,    dibenzyl ether,    dibutyl carbonate,    dibutyl hydrogen phosphite,    diethyl ether,    diethylene glycol dibutyl ether,    dihexyl ether,    diisopropylamine,    dipentylamine,    ethanol,    ethyl benzoate,    ethyl chloroacetate,    ethyl phenylacetate,    heptyl acetate,    hexanenitrile,    trans-ethyl cinnamate,    tributyl phosphate,    trichloromethane,    triethyl phosphate,    triethylene glycol

Isomers

2-ethynylanisole
Molecular structure of 2-ethynylanisole
3-ethynylanisole
Molecular structure of 3-ethynylanisole
4-ethynylbenzyl alcohol
Molecular structure of 4-ethynylbenzyl alcohol
1-ethynyl-4-methoxybenzene
Molecular structure of 1-ethynyl-4-methoxybenzene
1-indanone
Molecular structure of 1-indanone
2-indanone
Molecular structure of 2-indanone
2-methylbenzofuran
Molecular structure of 2-methylbenzofuran
4-methylbenzofuran
Molecular structure of 4-methylbenzofuran
5-methylbenzofuran
Molecular structure of 5-methylbenzofuran
7-methyl-1-benzofuran
Molecular structure of 7-methyl-1-benzofuran
2-methylbicyclo[4.2.0]octa-1,3,5-trien-7-one
Molecular structure of 2-methylbicyclo[4.2.0]octa-1,3,5-trien-7-one
3-methylbicyclo[4.2.0]octa-1,3,5-trien-7-one
Molecular structure of 3-methylbicyclo[4.2.0]octa-1,3,5-trien-7-one
4-methylbicyclo[4.2.0]octa-1,3,5-trien-7-one
Molecular structure of 4-methylbicyclo[4.2.0]octa-1,3,5-trien-7-one
phenyl propargyl ether
Molecular structure of phenyl propargyl ether
2-phenylprop-2-enal
Molecular structure of 2-phenylprop-2-enal
(E)-3-phenyl-2-propenal
Molecular structure of (E)-3-phenyl-2-propenal
1-phenylprop-2-en-1-one
Molecular structure of 1-phenylprop-2-en-1-one
1-phenyl-2-propyn-1-ol
Molecular structure of 1-phenyl-2-propyn-1-ol
3-phenyl-2-propyn-1-ol
Molecular structure of 3-phenyl-2-propyn-1-ol
3-vinylbenzaldehyde
Molecular structure of 3-vinylbenzaldehyde