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CAS No 532-11-6 , 5-(4-methoxyphenyl)dithiole-3-thione

  • Name: 5-(4-methoxyphenyl)dithiole-3-thione
  • Synonyms: Halpen; Felviten; Mucinol; Sulfarlem; Heporal; 532-11-6;anetholtrithion;5-(4-methoxyphenyl)dithiole-3-thione; Tiotrifar; Tiopropen;
  • CAS Registry Number:
  • Density: 1.41g/cm3
  • Refractive index: 1.732
  • Safety Statements: Poison by intramuscular route. Moderately toxic by ingestion and intraperitoneal routes. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of SOx.
  • EINECS: 208-528-5
  • Molecular Weight: 240.36492
  • InchiKey: KYLIZBIRMBGUOP-UHFFFAOYSA-N
  • InChI: InChI=1S/C10H8OS3/c1-11-8-4-2-7(3-5-8)9-6-10(12)14-13-9/h2-6H,1H3
  • Molecular Formula: C10H8OS3
  • Molecular Structure:CAS No:532-11-6 5-(4-methoxyphenyl)dithiole-3-thione

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References of 5-(4-methoxyphenyl)dithiole-3-thione
Title: Anethole Trithione
CAS Registry Number: 532-11-6
CAS Name: 5-(4-Methoxyphenyl)-3H-1,2-dithiole-3-thione
Synonyms: 3-(p-anisyl)trithione; 3-(p-methoxyphenyl)-4,5-dithiacyclopent-2-ene-1-thione; trithio-p-methoxyphenylpropene; 5-(p-methoxyphenyl)-1,2-dithiacyclopent-4-ene-3-thione; 3-(p-methoxyphenyl)trithione; trithioanethole; anethole dithiolthione; ADT
Trademarks: Felviten (Grñenthal); Mucinol (Sanofi Winthrop); Sialor (Solvay); Sulfarlem (Solvay)
Molecular Formula: C10H8OS3
Molecular Weight: 240.36
Percent Composition: C 49.97%, H 3.35%, O 6.66%, S 40.02%
Literature References: Organosulfur compound that enhances glutathione synthesis and stimulates secretion of bile and saliva. Prepn: B. B?ttcher, A. Lüttringhaus, Ann. 557, 89 (1947); O. Gaudin, N. Lozac'h, Compt. Rend. 224, 557 (1947); A. Thuillier, J. Vialle, Bull. Soc. Chim. Fr. 1959, 1398. HPLC determn in urine: A. N. Masoud, E. Bueding, J. Chromatogr. 276, 111 (1983). Clinical trial in xerostomia: J. B. Epstein et al., Oral Surg. Oral Med. Oral Pathol. 56, 495 (1983). Clinical trial in chemoprevention of lung cancer: S. Lam et al., J. Natl. Cancer Inst. 94, 1001 (2002). Review of mechanism of chemoprotective and antioxidant effects: M.-O. Christen, Methods Enzymol. 252, 316-323 (1995).
Properties: Orange-colored prisms from butyl acetate. Very bitter taste. mp 111°. Practically insol in water. Sol in pyridine, chloroform, benzene, dioxane, carbon disulfide. Slightly sol in ether, acetone, ethyl acetate, acetic acid, alc, cyclohexane, petr ether.
Melting point: mp 111°
Therap-Cat: Choleretic; sialogogue.
Keywords: Choleretic; Sialagogue.