![]() | |
Names | |
---|---|
IUPAC name
(E)-3-phenylprop-2-enenitrile
| |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.015.957 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C9H7N | |
Molar mass | 129.162 g·mol−1 |
Density | 1.0374 (15.2 °C) |
Melting point | 22 °C (72 °F; 295 K) |
Boiling point | 263.8 °C (506.8 °F; 537.0 K) |
log P | 1.96 |
Hazards | |
GHS labelling: [1] | |
![]() ![]() | |
Danger | |
H301, H312, H317 | |
P261, P264, P270, P272, P280, P301+P316, P302+P352, P317, P321, P330, P333+P313, P362+P364, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
(E)-Cinnamonitrile is an organic compound approved for use as a fragrance in products such as air fresheners. [2] [3] It has a spicy cinnamon aroma.
Synthetic routes include an aldol-like condensation of benzaldehyde with acetonitrile under alkaline conditions, [4] an elimination reaction of various oximes derived from cinnamaldehyde, [5] and oxidative coupling of benzene to acrylonitrile. [6]
![]() | |
Names | |
---|---|
IUPAC name
(E)-3-phenylprop-2-enenitrile
| |
Other names
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.015.957 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C9H7N | |
Molar mass | 129.162 g·mol−1 |
Density | 1.0374 (15.2 °C) |
Melting point | 22 °C (72 °F; 295 K) |
Boiling point | 263.8 °C (506.8 °F; 537.0 K) |
log P | 1.96 |
Hazards | |
GHS labelling: [1] | |
![]() ![]() | |
Danger | |
H301, H312, H317 | |
P261, P264, P270, P272, P280, P301+P316, P302+P352, P317, P321, P330, P333+P313, P362+P364, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
(E)-Cinnamonitrile is an organic compound approved for use as a fragrance in products such as air fresheners. [2] [3] It has a spicy cinnamon aroma.
Synthetic routes include an aldol-like condensation of benzaldehyde with acetonitrile under alkaline conditions, [4] an elimination reaction of various oximes derived from cinnamaldehyde, [5] and oxidative coupling of benzene to acrylonitrile. [6]