Names | |
---|---|
Preferred IUPAC name
Anthracene-9-carbaldehyde | |
Other names
9-Anthraldehyde, 9-Anthracenaldehyde, Anthracene-9-carbaldehyde
| |
Identifiers | |
3D model (
JSmol)
|
|
639167 | |
ChemSpider | |
ECHA InfoCard | 100.010.349 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C15H10O | |
Molar mass | 206.244 g·mol−1 |
Appearance | yellow solid |
Melting point | 104 °C (219 °F; 377 K) |
Hazards | |
GHS labelling: | |
Warning | |
H302, H312, H315, H319, H332, H335 | |
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Anthracene-9-carbaldehyde is the most common monoaldehyde derivative of anthracene. It is a yellow solid that is soluble in common organic solvents. It is prepared by Vilsmeier formylation of anthracene. [1] [2] The compound is also used as a building block for supramolecular assemblies. [3] Hydrogenation of 9-anthracenecarboxaldehyde gives 9-anthracenemethanol.
Names | |
---|---|
Preferred IUPAC name
Anthracene-9-carbaldehyde | |
Other names
9-Anthraldehyde, 9-Anthracenaldehyde, Anthracene-9-carbaldehyde
| |
Identifiers | |
3D model (
JSmol)
|
|
639167 | |
ChemSpider | |
ECHA InfoCard | 100.010.349 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C15H10O | |
Molar mass | 206.244 g·mol−1 |
Appearance | yellow solid |
Melting point | 104 °C (219 °F; 377 K) |
Hazards | |
GHS labelling: | |
Warning | |
H302, H312, H315, H319, H332, H335 | |
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Anthracene-9-carbaldehyde is the most common monoaldehyde derivative of anthracene. It is a yellow solid that is soluble in common organic solvents. It is prepared by Vilsmeier formylation of anthracene. [1] [2] The compound is also used as a building block for supramolecular assemblies. [3] Hydrogenation of 9-anthracenecarboxaldehyde gives 9-anthracenemethanol.