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Gallacetophenone: Difference between revisions

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Revision as of 14:48, 12 June 2020 editFswitzer4 (talk \| contribs)Extended confirmed users11,001 editsm Added FDA UNII← Previous edit		Latest revision as of 09:27, 25 June 2022 edit undoBrownHairedGirl (talk \| contribs)Autopatrolled, Extended confirmed users, File movers, Pending changes reviewers, Rollbackers2,942,733 edits Cleanup 1 reference: convert <ref>URL {{webarchive}}</ref> to <ref>{{cite web}}</ref>. NB: title etc is missing, and will display error msgTag: AWB
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	'''Gallacetophenone''' is the ] derivative of ]. It can be synthesized from pyrogallol using ] and ].<ref>http://talkchem.com/synthetic-chemistry/gallacetophenone-synthesis-synthesis-of-gallacetophenone.html ~~{{webarchive~~ \|url=https://web.archive.org/web/20100116013814/http://talkchem.com/synthetic-chemistry/gallacetophenone-synthesis-synthesis-of-gallacetophenone.html \|date=January 16, 2010 }}</ref>		'''Gallacetophenone''' is the ] derivative of ]. It can be synthesized from pyrogallol using ] and ].<ref>{{cite web \|url=http://talkchem.com/synthetic-chemistry/gallacetophenone-synthesis-synthesis-of-gallacetophenone.html \|title= \|website=talkchem.com \|archive-url=https://web.archive.org/web/20100116013814/http://talkchem.com/synthetic-chemistry/gallacetophenone-synthesis-synthesis-of-gallacetophenone.html \|archive-date=January 16, 2010}}</ref>

	==References==		==References==
	{{reflist}}		{{reflist}}


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	{{Ketone-stub}}		{{Ketone-stub}}

Latest revision as of 09:27, 25 June 2022

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	528-21-2
3D model (JSmol)	Interactive image
ChemSpider	10256
ECHA InfoCard	100.007.665
PubChem CID	10706
UNII	C70E921C4P
CompTox Dashboard (EPA)	DTXSID2060179
InChI InChI=1S/C8H8O4/c1-4(9)5-2-3-6(10)8(12)7(5)11/h2-3,10-12H,1H3Key: XIROXSOOOAZHLL-UHFFFAOYSA-N InChI=1/C8H8O4/c1-4(9)5-2-3-6(10)8(12)7(5)11/h2-3,10-12H,1H3Key: XIROXSOOOAZHLL-UHFFFAOYAA
SMILES O=C(c1c(O)c(O)c(O)cc1)C
Properties
Chemical formula	C₈H₈O₄
Molar mass	168.148 g·mol
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 , 100 kPa). N verify (what is ?) Infobox references

Chemical compound

Gallacetophenone is the acetyl derivative of pyrogallol. It can be synthesized from pyrogallol using zinc chloride and acetic anhydride.

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)

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