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| (1S)-1,2,3,4-Tetrahydro-8-methoxy-1α,3β-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol Basic information |
Product Name: | (1S)-1,2,3,4-Tetrahydro-8-methoxy-1α,3β-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol | Synonyms: | Hamatine;6-Isoquinolinol, 5-(4,5-dimethoxy-2-methyl-1-naphthalenyl)-1,2,3,4- tetrahydro-8-methoxy-1,3-dimethyl-, (1S,3S,5R)-;(1S)-1,2,3,4-Tetrahydro-8-methoxy-1α,3β-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol | CAS: | 56688-90-5 | MF: | C25H29NO4 | MW: | 407.5 | EINECS: | | Product Categories: | | Mol File: | 56688-90-5.mol | |
| (1S)-1,2,3,4-Tetrahydro-8-methoxy-1α,3β-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol Chemical Properties |
Melting point | 250-2°C | Boiling point | 565.3±50.0 °C(Predicted) | density | 1.137±0.06 g/cm3(Predicted) | pka | 8.19±0.60(Predicted) |
| (1S)-1,2,3,4-Tetrahydro-8-methoxy-1α,3β-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol Usage And Synthesis |
Description | The roots of Ancistrocladus hamatus yield this alkaloid which forms colourless
needles when recrystallized from MeOH. The structure, as a naphthyl derivative
of tetrahydroisoquinoline has been established from spectroscopic data. | Definition | ChEBI: Ancistrocladine is a member of isoquinolines and a member of naphthalenes. | References | Govindachari et al., Ind. 1. Chem., 13,641 (1975) |
| (1S)-1,2,3,4-Tetrahydro-8-methoxy-1α,3β-dimethyl-5-[(aR)-4,5-dimethoxy-2-methyl-1-naphthalenyl]isoquinoline-6-ol Preparation Products And Raw materials |
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