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CAS No 140111-52-0 , 7-Azabicyclo[2.2.1]heptane,2-(6-chloro-3-pyridinyl)-, (1R,2R,4S)- Search by region : Switzerland

  • Name: 7-Azabicyclo[2.2.1]heptane,2-(6-chloro-3-pyridinyl)-, (1R,2R,4S)-
  • Synonyms: (1R-exo)-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane; CMI 488; Epibatidine;7-Azabicyclo[2.2.1]heptane,2-(6-chloro-3-pyridinyl)-, (1R-exo)-;7-Azabicyclo[2.2.1]heptane,2-(6-chloro-3-pyridinyl)-, (1R,2R,4S)-; Alkaloid 208/210from Dendrobates; (+)-Epibatidine; (1R,2R,4S)-Epibatidine;
  • CAS Registry Number:
  • Flash Point: 157.4°C
  • Boiling Point: 336.7°Cat760mmHg
  • Density: 1.223g/cm3
  • Refractive index: 1.576
  • Flash Point: 157.4°C
  • Molecular Weight: 208.69
  • InChI: InChI=1/C11H13ClN2/c12-11-4-1-7(6-13-11)9-5-8-2-3-10(9)14-8/h1,4,6,8-10,14H,2-3,5H2/t8-,9+,10+/m1/s1
  • Molecular Formula: C11H13 Cl N2
  • Molecular Structure:CAS No:140111-52-0 7-Azabicyclo[2.2.1]heptane,2-(6-chloro-3-pyridinyl)-, (1R,2R,4S)-

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140111-52-0 (+/-)-exo-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1.]heptane hydrochloride

  • (+/-)-exo-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1.]heptane hydrochloride Epibatidine (+/-) (free base) (+/-)-EPIBATIDINE exo-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1.]heptane Epibatidine (R)-2-(6-Chloro-pyridin-3-yl)-7-aza-bicyclo[2.2.1]heptan...
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References of 7-Azabicyclo[2.2.1]heptane,2-(6-chloro-3-pyridinyl)-, (1R,2R,4S)-
Title: Epibatidine
CAS Registry Number: 140111-52-0
CAS Name: (1R,2R,4S)-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane
Molecular Formula: C11H13ClN2
Molecular Weight: 208.69
Percent Composition: C 63.31%, H 6.28%, Cl 16.99%, N 13.42%
Literature References: First naturally occurring non-opioid, organochlorine, alkaloid analgesic; isolated from skin of the Ecuadoran poison frog, Epipedobates tricolor. Isoln and structural determn: T. F. Spande et al., J. Am. Chem. Soc. 114, 3475 (1992). First natural product identified which contains the 7-azabicyclo[2.2.1]heptane ring system. Synthesis of (±)-form: C. A. Broka, Tetrahedron Lett. 1993, 3251.
Properties: Basic, relatively polar, colorless oil. uv max (methanol): 217 nm, shoulder 250-280 nm.
Absorption maximum: uv max (methanol): 217 nm, shoulder 250-280 nm