Home > Name List By 2 > 2,15-Dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione,13,26-dimethyl-, (1S,11R,13S,14S,24R,26S)-

CAS No 3463-92-1 , 2,15-Dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione,13,26-dimethyl-, (1S,11R,13S,14S,24R,26S)-

  • Name: 2,15-Dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione,13,26-dimethyl-, (1S,11R,13S,14S,24R,26S)-
  • Synonyms: (+)-Carpaine;[1S-(1R*,11S*,13R*,14R*,24S*,26R*)]-13,26-Dimethyl-2,15-dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione;2,15-Dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione,13,26-dimethyl-, (1S,11R,13S,14S,24R,26S)-;2,15-Dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione,13,26-dimethyl-, [1S-(1R*,11S*,13R*,14R*,24S*,26R*)]-; Carpaine (6CI,8CI);
  • CAS Registry Number:
  • Flash Point: 353°C
  • Boiling Point: 660°C at 760 mmHg
  • Density: 0.954g/cm3
  • Refractive index: 1.453
  • Flash Point: 353°C
  • EINECS: 222-414-2
  • Molecular Weight: 0
  • InChI: InChI=1/C28H50N2O4/c1-21-25-19-17-23(29-21)13-9-5-3-8-12-16-28(32)34-26-20-18-24(30-22(26)2)14-10-6-4-7-11-15-27(31)33-25/h21-26,29-30H,3-20H2,1-2H3/t21-,22-,23+,24+,25-,26-/m0/s1
  • Molecular Formula: C28H50 N2 O4
  • Molecular Structure:CAS No:3463-92-1 2,15-Dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione,13,26-dimethyl-, (1S,11R,13S,14S,24R,26S)-

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3463-92-1 Carpaine

  • Carpaine, Min 99%
  • China Finechemie Co., Ltd. [Manufacturer]
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References of 2,15-Dioxa-12,25-diazatricyclo[22.2.2.211,14]triacontane-3,16-dione,13,26-dimethyl-, (1S,11R,13S,14S,24R,26S)-
Title: Carpaine
CAS Registry Number: 3463-92-1
Molecular Formula: C28H50N2O4
Molecular Weight: 478.71
Percent Composition: C 70.25%, H 10.53%, N 5.85%, O 13.37%
Literature References: Found in Carica papaya L. and in Vasconcellosia hastata Caruel, Caricaceae. Isoln from papaya leaves: Greshoff, Mededeel. uit's Lands. Plant., Buitenzorg. No. 7, 5 (1890); Rapoport, Baldridge, J. Am. Chem. Soc. 73, 343 (1951). Reportedly causes bradycardia, CNS depression: Kakowski, Arch. Int. Pharm. 15, 84 (1905). Structure and stereochemistry: Govindachari et al., Tetrahedron Lett. 1965, 1907. Absolute configuration: Coke, Rice, J. Org. Chem. 30, 3420 (1965). Review of structural studies: Govindachari, J. Indian Chem. Soc. 45, 945 (1968).
Properties: Monoclinic prisms from acetone, mp 119-120°. Sublimes at 120° under 0.05 mm pressure. [a]D12 +24.7° (c = 1.07 in ethanol). Slightly sol in water. Sol in most organic solvents except petr ether.
Melting point: mp 119-120°
Optical Rotation: [a]D12 +24.7° (c = 1.07 in ethanol)