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| (1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one Basic information |
Product Name: | (1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one | Synonyms: | 6-Oxabicyclo[3.2.1]octan-7-one, 4-bromo-, (1S-exo)- (9CI);Edoxaban Impurity 80;(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-oneQ: What is
(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one Q: What is the CAS Number of
(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one;(1S,4S,5S)-4-bromo-6-oxabicyclo[3.2.1]octan-7-one | CAS: | 139893-81-5 | MF: | C7H9BrO2 | MW: | 205.05 | EINECS: | | Product Categories: | | Mol File: | 139893-81-5.mol | ![(1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one Structure](CAS/20200515/GIF/139893-81-5.gif) |
| (1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one Chemical Properties |
Boiling point | 324.2±25.0 °C(Predicted) | density | 1.642±0.06 g/cm3(Predicted) | InChI | InChI=1/C7H9BrO2/c8-5-2-1-4-3-6(5)10-7(4)9/h4-6H,1-3H2/t4-,5?,6?/s3 | InChIKey | HIEDNXSBEYNHJB-OGAAFCRYNA-N | SMILES | [C@]12([H])CC(OC1=O)C(Br)CC2 |&1:0,r| |
| (1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one Usage And Synthesis |
Uses | Used as Edoxaban impurity. | Synthesis | (1S)-Cyclohex-3-ene-1-carboxylic acid (II) (5 g) was dissolved in dichloromethane (25 mL). To this solution, N-bromosuccinimide (1.1 mole) was added at room temperature. In two lots, calcium oxide (0.25 mole) was charged to the Suspension. The reaction mixture was stirred at 20 to 25°C for 1 hour and filtered. The bed was washed with dichloromethane (10 mL). The washings were combined with the filtrate, and the solvent was recovered under vacuum at 35 to 40 °C. Deionized water (50 mL) was charged to the solid, heated to 50 °C, stirred for 10 minutes, and filtered. The bed was washed with deionized water (10 mL) and suction dried. The solid was dried under vacuum at 45-50 °C to get (1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one. Yield: 61% |
| (1S,4S,5S)-4-Bromo-6-oxabicyclo[3.2.1]octan-7-one Preparation Products And Raw materials |
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