(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one
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Product Name:
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(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one |
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Synonyms:
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6-Oxabicyclo[3.2.1]octan-7-one,4-bromo-,(1S-exo)-(9CI);(1S,4S,5S)-4-bromo-6-oxabicyclo[3.2.1]octan-7-one;EdoxabanImpurity80;(1S,4S,5S)-4-Bromo-6-oxabiChemicalbookcyclo[3.2.1]octan-7-oneQ:Whatis(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-oneQ:WhatistheCASNumberof(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one |
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CAS:
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139893-81-5 |
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MF:
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C7H9BrO2 |
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MW:
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205.05 |
(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one
| Density | 1.642±0.06 g/cm3(Predicted) |
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Boiling Point:
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324.2±25.0 °C(Predicted) |
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Solubility
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Slightly soluble in water, soluble in DMSO/methanol. |
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Form
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solid
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Color
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White |
Usage
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Uses
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(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one is mainly used in the field of pharmaceutical intermediates. It is a key intermediate for the synthesis of edoxaban, a new type of oral anticoagulant. In the synthesis process of edoxaban, it can be used to prepare tert-butyl (1R,2S,5S)-2-amino-5-(dimethylcarbamoyl)cyclohexylcarbamate, a key intermediate of edoxaban, through a series of reactions such as ring opening, oxidation, and enzyme-catalyzed asymmetric reductive amination. In addition, it can also serve as a starting material for the preparation of other biologically active heterocyclic compounds, and has important application value in organic synthesis and drug research and development.
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