Gallacetophenone
Names | |
---|---|
Preferred IUPAC name 1-(2,3,4-Trihydroxyphenyl)ethan-1-one | |
Other names 1-(2,3,4-Trihydroxyphenyl)ethanone Alizarin Yellow C Galloacetophenone 2',3',4'-Trihydroxyacetophenone | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChemSpider |
|
ECHA InfoCard | 100.007.665 |
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C8H8O4 |
Molar mass | 168.148 g·mol−1 |
Melting point | 171 to 172 °C (340 to 342 °F; 444 to 445 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references |
Chemical compound
Gallacetophenone is the acetyl derivative of pyrogallol. It can be synthesized from pyrogallol using zinc chloride and acetic anhydride.[1]
References
- ^ talkchem.com https://web.archive.org/web/20100116013814/http://talkchem.com/synthetic-chemistry/gallacetophenone-synthesis-synthesis-of-gallacetophenone.html. Archived from the original on January 16, 2010.
{{cite web}}
: Missing or empty|title=
(help)
- v
- t
- e