Carboxin
Structural Formula Vector Image
Title: Carboxin
CAS Registry Number: 5234-68-4
CAS Name: 5,6-Dihydro-2-methyl-N-phenyl-1,4-oxathiin-3-carboxamide
Additional Names: 2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiin; carbathiin; DCMO
Trademarks: Vitavax (Uniroyal)
Molecular Formula: C12H13NO2S
Molecular Weight: 235.30
Percent Composition: C 61.25%, H 5.57%, N 5.95%, O 13.60%, S 13.63%
Literature References: Systemic fungicide, effective against loose smut in cereals. Prepn: B. von Schmeling et al., US 3249499 (1966 to U.S. Rubber); M. Kulka et al., US 3393202 (1968 to Uniroyal). Fungicidal activity: B. von Schmeling, M. Kulka, Science 152, 659 (1966). Inhibitor of succinate oxidation: D. E. Mathre, Phytopathology 60, 671 (1970); G. A. White, Biochem. Biophys. Res. Commun. 44, 1212 (1971); P. C. Mowery et al., ibid. 71, 354 (1976). Residue determn in crops: J. R. Lane, J. Agric. Food Chem. 18, 409 (1970); H. R. Sisken, J. E. Newell, ibid. 19, 738 (1971). Toxicity studies: T. V. Dyadicheva, Gig. Tr. Prof. Zabol. 1979(2), 55, C.A. 90, 146673b (1979).
Properties: Crystals, from ethanol or methanol, mp 93-95°. LD50 in rats, mice (mg/kg): 430, 3200 orally (Dyadicheva).
Melting point: mp 93-95°
Toxicity data: LD50 in rats, mice (mg/kg): 430, 3200 orally (Dyadicheva)
Use: Systemic plant fungicide.

Other Monographs:
SulfabenzamideNitrofenIndigoHQNO
PhenserineEthyl PhenylacetatePodophyllotoxinCresols
5-Bromoanthranilic AcidEvan's BlueViburnum prunifoliumAngostura Bark
NarasinBuserelinDipicrylamineFosfosal
©2006-2023 DrugFuture->Chemical Index Database