Acetarsol

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Acetarsol
Kekulé, skeletal formula of acetarsol
Names
Preferred IUPAC name
Acetarsone[citation needed]
Systematic IUPAC name
(3-Acetamido-4-hydroxyphenyl)arsonic acid[1]
Other names
3-Acetamido-4-hydroxyphenylarsonic acid[citation needed]
Identifiers
97-44-9 N
ChEMBL ChEMBL1330792 N
ChemSpider 1908 YesY
EC Number 202-582-3
Jmol 3D model Interactive image
Interactive image
KEGG D07110 YesY
MeSH Acetarsol
PubChem 1985
UNII 806529YU1N YesY
UN number 3465
  • InChI=1S/C8H10AsNO5/c1-5(11)10-7-4-6(9(13,14)15)2-3-8(7)12/h2-4,12H,1H3,(H,10,11)(H2,13,14,15) YesY
    Key: ODFJOVXVLFUVNQ-UHFFFAOYSA-N YesY
  • InChI=1/C8H10AsNO5/c1-5(11)10-7-4-6(9(13,14)15)2-3-8(7)12/h2-4,12H,1H3,(H,10,11)(H2,13,14,15)
    Key: ODFJOVXVLFUVNQ-UHFFFAOYAX
  • CC(=O)Nc1cc(ccc1O)[As](O)(O)=O
  • CC(=O)NC1=CC(=CC=C1O)[As](O)(O)=O
Properties
C8H10AsNO5
Molar mass 275.0903 g mol−1
Pharmacology
ATC code A07AX02
G01AB01, P01CD02, P51AD05
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Acetarsol is an anti-infective.[2]

It was first discovered in 1921 at Pasteur Institute by Ernest Fourneau, and sold under the brand name Stovarsol (fourneau is the French word for stove).[3][4]

It has been given in suppositories.[5]

References

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  3. Éric Fouassier, Ces poisons qui guérissent, oct. 1996, p. 5.
  4. Traité de chimie organique, sous la direction de Victor Grignard, Paul Baud, vol. 22, Masson, 1959, p. 1127-1130.
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