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529-78-2

529-78-2 Structure

529-78-2 Structure
IdentificationBack Directory
[Name]

1,5-Methano-8H-pyrido(1,2-a)(1,4)diazocin-8-one, 3-(3-butenyl)-1,2,3,4 ,5,6-hexahydro-, (1R)-
[CAS]

529-78-2
[Synonyms]

Rhombifolin
rhombifoline
(1R)-3-(3-Butenyl)-1,2,3,4,5,6-hexahydro-1α,5α-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one
1,5-Methano-8H-pyrido(1,2-a)(1,4)diazocin-8-one, 3-(3-butenyl)-1,2,3,4 ,5,6-hexahydro-, (1R)-
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 3-(3-buten-1-yl)-1,2,3,4,5,6-hexahydro-, (1R,5S)-
[Molecular Formula]

C15H20N2O
[MDL Number]

MFCD34167512
[MOL File]

529-78-2.mol
[Molecular Weight]

244.33
Chemical PropertiesBack Directory
[Boiling point ]

120 °C(Press: 0.2 Torr)
[density ]

1.14±0.1 g/cm3(Predicted)
[form ]

Liquid
[pka]

9.45±0.20(Predicted)
[color ]

Light yellow to light brown
Hazard InformationBack Directory
[Description]

A minor alkaloid obtained from Thermopsis rhombifolia (Watt), Richards, the base was originally given the empirical formula ClsH2002N2, but subsequently changed to that given. It is strongly laevorotatory with [α]25D - 232.4° (c 2.13, EtOH) and yields crystalline salts including the hydrochloride, m.p. 256-8°C (dec.) which sublimes at l20°CjO.000l mm; the perchlorate, m.p. 243-5°C (dec.); platinichloride, m.p. 268° C and the picrate, m.p. 226°C (dec.).
[References]

Manske, Marion., Can. J. Res., 20B, 265 (1942)
Manske, Marion., ibid, 21B, 144 (1943)
Cockburn, Marion., Can. J. Chem., 30,92 (1952)
van Tamelen, Baran.,J. Amer. Chem. Soc., 71,4944 (1955)
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