PROFILPELAJAR.COM

Fluoroaspirin^[1]
Names
	Preferred IUPAC name 2-[(Fluoroacetyl)oxy]benzoic acid
	Other names Fluoroacetylsalicylic acid,; O-(Fluoroacetyl)salicylic acid
Identifiers
CAS Number	364-71-6;
3D model (JSmol)	Interactive image;
ChemSpider	61085;
PubChem CID	67766;
UNII	55RH7BA96P ;
CompTox Dashboard (EPA)	DTXSID30957750;
	InChI InChI=1S/C9H7FO4/c10-5-8(11)14-7-4-2-1-3-6(7)9(12)13/h1-4H,5H2,(H,12,13) Key: ISJRKJAXVBVDDK-UHFFFAOYSA-N;
	SMILES c1ccc(c(c1)C(=O)O)OC(=O)CF;
Properties
Chemical formula	C9H7FO4
Molar mass	198.149 g·mol−1
Hazards
	Lethal dose or concentration (LD, LC):
LD50 (median dose)	15 mg/kg (mice, subcutaneous)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Fluoroaspirin is the fluoroacetate ester of salicylic acid. It is the fluoroacetate analog of aspirin. Like other fluoroacetate esters, fluoroaspirin is highly toxic.^[2]

References

^ Saunders, BC (1957). Some aspects of the chemistry and toxic action of organic compounds containing phosphorus and fluorine (PDF).
^ Saunders, B. C.; Stacey, G. J. (1948). "358. Toxic fluorine compounds containing the C–F link. Part I. Methyl Fluoroacetate and Related Compounds". J. Chem. Soc. 70: 1773–1779. doi:10.1039/JR9480001773. PMID 18106001.

This article about an ester is a stub. You can help Wikipedia by expanding it.

[1] Saunders, BC (1957). Some aspects of the chemistry and toxic action of organic compounds containing phosphorus and fluorine (PDF).

[2] Saunders, B. C.; Stacey, G. J. (1948). "358. Toxic fluorine compounds containing the C–F link. Part I. Methyl Fluoroacetate and Related Compounds". J. Chem. Soc. 70: 1773–1779. doi:10.1039/JR9480001773. PMID 18106001.

[1]

[2]

Fluoroaspirin

See also

References