Name | tert-butyl 5-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylate |
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Synonyms |
2-t-butoxycarbonyl-5-hydroxy-1,2,3,4-tetrahydroisoquinoline
2(1H)-Isoquinolinecarboxylic acid, 3,4-dihydro-5-hydroxy-, 1,1-dimethylethyl ester tert-butyl 5-hydroxy-1,2,3,4-tetrahydroisoquinoline-2-carboxylate 2-tert-butoxycarbonyl-5-hydroxy-tetrahydroisoquinoline 2-Methyl-2-propanyl 5-hydroxy-3,4-dihydro-2(1H)-isoquinolinecarboxylate 5-hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester 2-tert-butyloxycarbonyl-5-hydroxy-1,2,3,4-tetrahydroisoquinoline tert-Butyl 5-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 378.6±42.0 °C at 760 mmHg |
Molecular Formula | C14H19NO3 |
Molecular Weight | 249.306 |
Flash Point | 182.7±27.9 °C |
Exact Mass | 249.136490 |
PSA | 49.77000 |
LogP | 2.21 |
Vapour Pressure | 0.0±0.9 mmHg at 25°C |
Index of Refraction | 1.558 |
Hazard Codes | Xi |
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HS Code | 2933499090 |
~59% 216064-48-1 |
Literature: Takeda Chemical Industries, Ltd. Patent: EP1123918 A1, 2001 ; |
~79% 216064-48-1 |
Literature: Watanabe, Toshihiro; Kinoyama, Isao; Takizawa, Kenji; Hirano, Seiko; Shibanuma, Tadao Chemical and Pharmaceutical Bulletin, 1999 , vol. 47, # 5 p. 672 - 677 |
~83% 216064-48-1 |
Literature: Fray, M. Jonathan; Allen, Paul; Bradley, Paul R.; Challenger, Clare E.; Closier, Michael; Evans, Tim J.; Lewis, Mark L.; Mathias, John P.; Nichols, Carly L.; Po-Ba, Yvonne M.; Snow, Hayley; Stefaniak, Mark H.; Vuong, Hannah V. Tetrahedron, 2006 , vol. 62, # 29 p. 6869 - 6875 |
~% 216064-48-1 |
Literature: Bioorganic and Medicinal Chemistry Letters, , vol. 16, # 24 p. 6293 - 6297 |
~% 216064-48-1 |
Literature: Tetrahedron Letters, , vol. 38, # 49 p. 8569 - 8572 |
Precursor 5 | |
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DownStream 0 |
HS Code | 2933499090 |
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Summary | 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |