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CAS No 6159-55-3 , Vasicine Search by region : China

  • Name: Vasicine
  • Synonyms: Vasicine;(R)-1,2,3,9-Tetrahydropyrrolo[2,1-b]quinazolin-3-ol;-;
  • CAS Registry Number:
  • Transport: 1544
  • Melting Point: 182 ºC
  • Density: 1.37 g/cm3
  • Refractive index: 1.709
  • Safety Statements: Poison by ingestion, intraperitoneal, and subcutaneous routes. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.
  • EINECS: 228-180-8
  • Molecular Weight: 188.23
  • InChI: InChI=1/C11H12N2O/c14-10-5-6-13-7-8-3-1-2-4-9(8)12-11(10)13/h1-4,10,14H,5-7H2/t10-/m0/s1
  • Molecular Formula: C11H12N2O
  • Molecular Structure:CAS No:6159-55-3 Vasicine

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6159-55-3 VASICINE

  • China Nanjing Chemlin Chemical Industry Co.,Ltd. [Manufacturer]
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  • Address: Rm.902 Longyin Plaza,
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    (N)Nanjing 210009,China null,nullChina
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6159-55-3 vasicine

  • China YiPeng Chemical [Manufacturers]
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6159-55-3 vasicine

  • China BioBioPha Co., Ltd. [Manufacturer]
  • Tel: +86-871-5217109
  • Fax: +86-871-5217109
  • Address: 132 Lanhei Road, Kunming Institute of Botany, Chinese Academy of Sciences null,nullChina
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References of Vasicine
Title: Vasicine
CAS Registry Number: 6159-55-3
CAS Name: 1,2,3,9-Tetrahydropyrrolo[2,1-b]quinazolin-3-ol
Synonyms: peganine
Molecular Formula: C11H12N2O
Molecular Weight: 188.23
Percent Composition: C 70.19%, H 6.43%, N 14.88%, O 8.50%
Literature References: Isoln from Adhatoda vasica Nees, Acanthaceae: Hooper, Pharm. J. 18, 841 (1888); Sen, Ghose, J. Indian Chem. Soc. 1, 315 (1924); Mehta et al., J. Org. Chem. 28, 445 (1963). Isoln from Peganum harmala L., Zygophyllaceae: Sp?th, Nikawitz, Ber. 67, 45 (1934); Sp?th, Kuffner, ibid. 67, 868 (1934). Structure and synthesis: Sp?th et al., ibid. 68, 699 (1935); Sp?th, Platzer, ibid. 69, 255 (1936). Synthesis of dl-vasicine: Southwick, Casanova, J. Am. Chem. Soc. 80, 1168 (1958). Reviews: Sp?th, Monatsh. Chem. 72, 115 (1938); H. T. Openshaw, "The Quinazoline Alkaloids" in The Alkaloids vol. III, R. H. F. Manske, H. L. Holmes, Eds. (Academic Press, New York, 1953) pp 101-118; Ray, J. Indian Chem. Soc. 35, 697 (1958).
 
Derivative Type: dl-Form
Properties: Needles from alc. mp 210°. Sublimes in high vacuum. Sol in acetone, alcohol, chloroform; slightly sol in water, ether, benzene.
Melting point: mp 210°
 
Derivative Type: l-Form
Properties: Needles from alc, mp 212°. [a]D14 -254° (c = 2.4 in CHCl3); [a]D14 -62° (c = 2.4 in alc). In dil HCl this alkaloid is dextrorotatory.
Melting point: mp 212°
Optical Rotation: [a]D14 -254° (c = 2.4 in CHCl3); [a]D14 -62° (c = 2.4 in alc)
 
Derivative Type: Hydrochloride dihydrate
Properties: Needles, mp 208° (dry).
Melting point: mp 208° (dry)
 
Derivative Type: Hydriodide dihydrate
Properties: Needles, mp 195° (dry).
Melting point: mp 195° (dry)
 
Derivative Type: Methiodide
Properties: Needles from methanol, mp 187°.
Melting point: mp 187°
 
Derivative Type: Acetylvasicine
Molecular Formula: C11H11N2OCOCH3
Molecular Weight: 230.26
Percent Composition: C 67.81%, H 6.13%, N 12.17%, O 13.90%
Properties: Crystals, mp 123°, bp0.01 230-240°.
Melting point: mp 123°
Boiling point: bp0.01 230-240°