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CAS No 2398-96-1 , O-naphthalen-2-yl N-methyl-N-(3-methylphenyl)carbamothioate

  • Name: O-naphthalen-2-yl N-methyl-N-(3-methylphenyl)carbamothioate
  • Synonyms: Chinofungin;O-naphthalen-2-yl N-methyl-N-(3-methylphenyl)carbamothioate; Tonoftal;Tinactin; Tinaderm; Sporiline; Tolnaphthate; Dermoxin; Aftate; Tolsanil;
  • CAS Registry Number:
  • Transport: 25kgs
  • Melting Point: 110.5-111.5 ºC
  • Density: 1.223 g/cm3
  • Refractive index: 1.697
  • Water Solubility: <0.1 G/100 ML AT 22 ºC
  • EINECS: 219-266-6
  • Molecular Weight: 307.40938
  • InchiKey: FUSNMLFNXJSCDI-UHFFFAOYSA-N
  • InChI: InChI=1S/C19H17NOS/c1-14-6-5-9-17(12-14)20(2)19(22)21-18-11-10-15-7-3-4-
    8-16(15)13-18/h3-13H,1-2H3
  • Molecular Formula: C19H17NOS
  • Molecular Structure:CAS No:2398-96-1 O-naphthalen-2-yl N-methyl-N-(3-methylphenyl)carbamothioate

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References of O-naphthalen-2-yl N-methyl-N-(3-methylphenyl)carbamothioate
Title: Tolnaftate
CAS Registry Number: 2398-96-1
CAS Name: Methyl(3-methylphenyl)carbamothioic acid O-2-naphthalenyl ester
Synonyms: m,N-dimethylthiocarbanilic acid O-2-naphthyl ester; O-2-naphthyl m,N-dimethylthiocarbanilate; 2-naphthyl N-methyl-N-(3-tolyl)thionocarbamate
Manufacturers' Codes: Sch-10144
Trademarks: Aftate (Schering-Plough); Chinofungin (Chinoin); Fungistop (Essex); Hi-Alarzin (Yamanouchi); Sporiline (Schering-Plough); Timoped (Reckitt & Colman); Tinactin (Schering-Plough); Tinaderm (Schering-Plough); Tonoftal (Essex)
Molecular Formula: C19H17NOS
Molecular Weight: 307.41
Percent Composition: C 74.23%, H 5.57%, N 4.56%, O 5.20%, S 10.43%
Literature References: Prepn: FR 1337797; Miyazaki et al., US 3334126 (1963, 1967 to Japan Soda); Noguchi et al., J. Pharm. Soc. Jpn. 88, 335 (1968). Pharmacology and toxicology: Noguchi et al., Antimicrob. Agents Chemother. 1962, 259; Hashimoto et al., Toxicol. Appl. Pharmacol. 8, 380 (1966); Noguchi et al., ibid. 368. Clinical comparison with undecylenic acid: J. F. Fuerst et al., Cutis 25, 544 (1980); F. Battistini et al., Int. J. Dermatol. 22, 388 (1983). Mode of action study: M. P. Gupta et al., J. Vet. Med. Mycol. 29, 45 (1991). LC determn in pharmaceuticals: A. K. Dash, J. Pharm. Biomed. Anal. 11, 847 (1993). Comprehensive description: idem, Anal. Profiles Drug Subs. Excip. 23, 543-570 (1994).
Properties: Crystals from alcohol, mp 110.5-111.5°. Practically insol in water. Sparingly sol in methanol, ethanol. Sol in chloroform (1:1.5), acetone (1:7), CCl4 (1:9). uv max (methanol): 258, 222 nm. LD50 in mice, rats (g/kg): >10, >6 orally; >6, >4 s.c. (Hashimoto).
Melting point: mp 110.5-111.5°
Absorption maximum: uv max (methanol): 258, 222 nm
Toxicity data: LD50 in mice, rats (g/kg): >10, >6 orally; >6, >4 s.c. (Hashimoto)
Therap-Cat: Antifungal.
Therap-Cat-Vet: Antifungal.
Keywords: Antifungal (Synthetic); Thiocarbamates.