Decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydropyridin-2-yl)quinoline
- Product Name
- Decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydropyridin-2-yl)quinoline
- CAS No.
- 6887-36-1
- Chemical Name
- Decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydropyridin-2-yl)quinoline
- Synonyms
- Lobinaline;Decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydropyridin-2-yl)quinoline;Quinoline, decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydro-2-pyridinyl)-, (4aR,5R,6R,7S,8aR)-
- CBNumber
- CB92319804
- Molecular Formula
- C27H34N2
- Formula Weight
- 386.57
- MOL File
- 6887-36-1.mol
More
Less
Decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydropyridin-2-yl)quinoline Property
- Melting point:
- 94-5°C
- Boiling point:
- 522.6±50.0 °C(Predicted)
- Density
- 1.14±0.1 g/cm3(Predicted)
- pka
- 9.81±0.70(Predicted)
More
Less
Decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydropyridin-2-yl)quinoline Chemical Properties,Usage,Production
Description
This alkaloid was first isolated by Manske from Lobelia cardinalis L. It crystallizes with difficulty from EtOH yielding colourless prisms and has [o:l54 + 22.3° (CHCI 3). The hydrochloride sesquihydrate has m.p. 220°C. Oxidation of the alkaloid with KMn04 yields benzoic acid. Pharmacologically, the alkaloid shows few, if any, of the typical characteristics of lobeline (q.v.).
References
Manske., Can. 1. Res., 16B, 445 (1938)
Pharmacology:
See pharmacological note made by Unna in the above reference.
Biosynthesis:
Gupta, Spenser., Chern. Commull., 893 (1966)
Decahydro-1-methyl-5,7-diphenyl-6-(3,4,5,6-tetrahydropyridin-2-yl)quinoline Preparation Products And Raw materials
Raw materials
Preparation Products
More
Less