![]() | |
Names | |
---|---|
IUPAC name
2-hydroxy-4-(2-hydroxy-4-methoxy-3,6-dimethylbenzoyl)oxy-6-methylbenzoic acid
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C18H18O7 | |
Molar mass | 346.335 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Ramalic acid is an organic compound with the molecular formula C18H18O7. [1] [2] Ramalic acid occurs as a secondary metabolite in some lichens like Ramalina pollinaria wherfrom ramalic acid has its name. [3] [4] [5] [6] Ramalic acid can be used as a dye. [6]
{{
cite journal}}
: Cite journal requires |journal=
(
help)
![]() | |
Names | |
---|---|
IUPAC name
2-hydroxy-4-(2-hydroxy-4-methoxy-3,6-dimethylbenzoyl)oxy-6-methylbenzoic acid
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C18H18O7 | |
Molar mass | 346.335 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Ramalic acid is an organic compound with the molecular formula C18H18O7. [1] [2] Ramalic acid occurs as a secondary metabolite in some lichens like Ramalina pollinaria wherfrom ramalic acid has its name. [3] [4] [5] [6] Ramalic acid can be used as a dye. [6]
{{
cite journal}}
: Cite journal requires |journal=
(
help)