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CAS No 485-35-8 , Cytisine

  • Name: Cytisine
  • Synonyms: 1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 1,2,3,4,5,6-hexahydro-, (1R-cis)-; 1,5-Methano-8H-pyrido(1,2-a)(1,5)diazocin-8-one, 1,2,3,4,5,6-hexahydro-; 1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 1,2,3,4,5,6-hexahydro-, (1R)-; 1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one;(1R,5S)-1,2,3,4,5,6-Hexahydro-1,5-methanopyrido[1,2-a][1,5]diazocin-8-one; 2-a)(1,5)diazocin-8-one,1,2,3,4,5,6-hexahydro-5-methano-8h-pyrido(1;Cytisine; 1,2,3,4,5,6-Hexahydro-1,5-methano-pyrido[1,2-a][1,5]diazocin; 5)diazocin-8-one,1,2,3,4,5,6-hexahydro-5-methano-8h-pyrido((1r)-2-a)(1;(-)-cytisine ; SOPHORINE;
  • CAS Registry Number:
  • Transport: UN 2811
  • Melting Point: 154-156 ºC
  • Boiling Point: 218 ºC (2 MMHG)
  • Density: 1.24 g/cm3
  • Water Solubility: Soluble to 100 mM in Water
  • Safety Statements: R25;R36/37/38
  • Hazard Symbols: T: Toxic;
  • EINECS: 207-616-0
  • Molecular Weight: 190.24
  • InChI: InChI=1/C11H14N2O/c14-11-3-1-2-10-9-4-8(5-12-6-9)7-13(10)11/h1-3,8-9,12H,4-7H2/t8?,9-/m1/s1
  • Risk Statements: S26;S28;S36/37;S45
  • Molecular Formula: C11H14N2O
  • Molecular Structure:CAS No:485-35-8 Cytisine

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485-35-8 CYTISINE

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485-35-8 Cytisine

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485-35-8 Temiverine

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485-35-8 CYTISINE(LABURNIN)(RG)

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485-35-8 7,11-diazatricyclo[7.3.1.0~2,7~]trideca-2,4-dien-6-one

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References of Cytisine
Title: Cytisine
CAS Registry Number: 485-35-8
CAS Name: (1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido-[1,2-a][1,5]diazocin-8-one
Synonyms: baptitoxine; sophorine; ulexine
Trademarks: Cytiton (USSR)
Molecular Formula: C11H14N2O
Molecular Weight: 190.24
Percent Composition: C 69.45%, H 7.42%, N 14.73%, O 8.41%
Literature References: Toxic principle in seed of Laburnum anagyroides Medik. and other Leguminosae. Extraction: Ing, J. Chem. Soc. 1931, 2200; Sp?th, Galinovsky, Ber. 65, 1526 (1932); 66, 1338 (1933); Lecoq, Bull. Soc. Chim. Fr. 10, 153 (1943). Structure: Ing, J. Chem. Soc. 1932, 2778. Synthesis: Bohlmann et al., Angew. Chem. 67, 708 (1955); Van Tamelen, Baran, J. Am. Chem. Soc. 77, 4944 (1955). Absolute configuration: Okuda et al., Chem. Ind. (London) 1961, 1751. Pharmacological properties: R. B. Barlow, L. J. McLeod, Br. J. Pharmacol. 35, 161 (1969).
Properties: Orthorhombic prisms from acetone, mp 152-153°. Sublimes. bp2 218°. [a]D17 -120°. pK1 6.11; pK2 13.08. Sol in 1.3 parts water, 13 parts acetone, 1.3 parts methanol, 3.5 parts alcohol, 30 parts benzene, 10 parts ethyl acetate, 2.0 parts chloroform. Practically insol in petr ether. LD50 in mice (mg/kg): 1.73 i.v.; 9.4 i.p.; 101 orally (Barlow, McLeod).
Melting point: mp 152-153°
Boiling point: bp2 218°
pKa: pK1 6.11; pK2 13.08
Optical Rotation: [a]D17 -120°
Toxicity data: LD50 in mice (mg/kg): 1.73 i.v.; 9.4 i.p.; 101 orally (Barlow, McLeod)
 
Derivative Type: Hydrochloride
Molecular Formula: C11H14N2O.HCl
Molecular Weight: 226.70
Percent Composition: C 58.28%, H 6.67%, N 12.36%, O 7.06%, Cl 15.64%
Properties: Deliquescent crystals, sol in water and alcohol. pH of 0.1 molar aq soln 4.3.
 
Derivative Type: Nitrate monohydrate
Molecular Formula: C11H14N2O.HNO3.H2O
Molecular Weight: 271.27
Percent Composition: C 48.70%, H 6.32%, N 15.49%, O 29.49%
Properties: Needles or leaflets, [a]D -81.5°. Sol in water, slightly sol in alcohol. Practically insol in ether.
Optical Rotation: [a]D -81.5°