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Energy Chemical |
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6,7-Dimethoxyisoquinoline manufacturers
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| | 6,7-Dimethoxyisoquinoline Basic information |
| Product Name: | 6,7-Dimethoxyisoquinoline | | Synonyms: | 6,7-Dimethoxyisoquinoline 96%;6,7-DiMethoxyisoquinoline 9;6,7-Dimethoxyisoquinoline96%;backebergine;6,7-Dimethoxyisoquinoline>Isoquinoline, 6,7-dimethoxy-;6,7-DIMETHOXYISOQUINOLINE ISO 9001:2015 REACH;6,7-Dimethoxyisoquinoline, 95%, HC-6011 | | CAS: | 15248-39-2 | | MF: | C11H11NO2 | | MW: | 189.21 | | EINECS: | | | Product Categories: | blocks;Heterocycles;Quinolines | | Mol File: | 15248-39-2.mol |  |
| | 6,7-Dimethoxyisoquinoline Chemical Properties |
| Melting point | 92.0 to 96.0 °C | | Boiling point | 158°C/0.9mmHg(lit.) | | density | 1.148±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Solid | | pka | 6.25±0.10(Predicted) | | color | White to Off-White | | CAS DataBase Reference | 15248-39-2 |
| Hazard Codes | Xi | | Hazard Note | Irritant | | HS Code | 2933499090 |
| | 6,7-Dimethoxyisoquinoline Usage And Synthesis |
| Uses | 6,7-Dimethoxyisoquinoline is used as an organocatalyst in the chemoselective O-tert-butoxycarbonylation of phenols. | | Definition | ChEBI: A member of the class of isoquinolines carrying two methoxy substituents at positions 6 and 7. | | Synthesis Reference(s) | Journal of the American Chemical Society, 79, p. 3773, 1957 DOI: 10.1021/ja01571a043 Synthesis, p. 288, 1974 Tetrahedron Letters, 13, p. 4789, 1972 |
| | 6,7-Dimethoxyisoquinoline Preparation Products And Raw materials |
| Raw materials | (2,2-Diethoxy-ethyl)-(3,4-dimethoxy-benzyl)-amine-->6,7-dimethoxy-2-[(4-methylphenyl)sulfonyl]-1,2,3,4-tetrahydroisoquinoline-->Ethanamine, N-[(3,4-dimethoxyphenyl)methylene]-2,2-diethoxy--->6,7-Dimethoxy-3,4-dihydro-2H-isoquinolin-1-one-->6,7-Dimethoxy-3,4-dihydroisoquinoline-->1-[(3,4-Dimethoxyphenyl)methyl]-3,4-dihydro-6,7-dimethoxyisoquinoline-->Veratraldehyde-->6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline-->PAPAVERINE-->6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride-->1,2-Dimethoxybenzene |
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