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CAS No 52-49-3 , 1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol Search by region : China

  • Name: 1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol
  • Synonyms: Paralest; Triesifenidile; Cyclodolum;hydrochloride; Triexifenidila; Tremin; Parcopane; Pacitane; Artane;Trihexyphenidyl hydrochloride;1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol; Benzhexol hydrochloride;
  • CAS Registry Number:
  • Transport: 3249
  • Melting Point: 258.5
  • Flash Point: 211°C
  • Boiling Point: 447.9°Cat760mmHg
  • Density: g/cm3
  • Safety Statements: Poison by ingestion, intraperitoneal, intravenous, and subcutaneous routes. An anticholinergic agent which causes human psychotropic effects. Human systemic effects by ingestion: distorted perceptions, eye effects, hallucinations, toxic psychosis. When heated to decomposition it emits very toxic fumes of NOx and HCl.
  • Hazard Symbols: Xn
  • Flash Point: 211°C
  • EINECS: 200-142-5
  • Molecular Weight: 337.92718
  • InchiKey: QDWJJTJNXAKQKD-UHFFFAOYSA-N
  • InChI: InChI=1S/C20H31NO.ClH/c22-20(18-10-4-1-5-11-18,
    19-12-6-2-7-13-19)14-17-21-15-8-3-9-16-21;/h1,4-5,10-11,19,22H,2-3,6-9,
    12-17H2;1H
  • Risk Statements: 22
  • Molecular Formula: C20H32ClNO
  • Molecular Structure:CAS No:52-49-3 1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol

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References of 1-cyclohexyl-1-phenyl-3-piperidin-1-ylpropan-1-ol
Title: Trihexyphenidyl Hydrochloride
CAS Registry Number: 52-49-3
CAS Name: a-Cyclohexyl-a-phenyl-1-piperidinepropanol hydrochloride
Synonyms: 3-(1-piperidyl)-1-cyclohexyl-1-phenyl-1-propanol hydrochloride; 1-phenyl-1-cyclohexyl-3-piperidyl-1-propanol hydrochloride; benzhexol chloride
Trademarks: Aparkane (ICN); Artane (Wyeth); Broflex (Bioglan); Cyclodol; Pacitane (Wyeth); Paralest (Parachemie); Pargitan (Abigo); Parkinane (Wyeth); Parkopan (Hexal); Peragit (AFI); Pipanol (Winthrop); Sedrena (Daiichi); Tremin (Schering-Plough); Triphedinon (Toho); Triphenidyl (Leciva); Tsiklodol
Molecular Formula: C20H32ClNO
Molecular Weight: 337.93
Percent Composition: C 71.08%, H 9.54%, Cl 10.49%, N 4.14%, O 4.73%
Literature References: Anticholinergic. Synthesis: Denton et al., J. Am. Chem. Soc. 71, 2053 (1949); Adamson, Wilkinson, US 2682543 (1954 to Burroughs Wellcome); Denton, US 2716121 (1955 to Am. Cyanamid). Resolution into isomers: Adamson, Duffin, GB 750156 (1956 to Wellcome Found.).
Properties: Crystals, dec 258.5°. Free base, mp 114.3-115.0°. Soly (g/100 ml): water at 25°, 1.0; alcohol 6; chloroform 5. More sol in methanol; very slightly sol in ether, benzene. pH of a 1% aq soln 5.5-6.0.
Melting point: Free base, mp 114.3-115.0°
 
Derivative Type: l-Form
Properties: Crystals from isopropyl alc, mp 264°. [a]D20 -30° (c = 0.4 in chloroform). Free base, mp 112-113°. [a]D20 -25° (c = 0.4 in ethanol).
Melting point: mp 264°; Free base, mp 112-113°
Optical Rotation: [a]D20 -30° (c = 0.4 in chloroform); [a]D20 -25° (c = 0.4 in ethanol)
 
Therap-Cat: Antiparkinsonian.
Keywords: Antiparkinsonian; Antimuscarinic.