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| (+)-B-METHOXYDIISOPINOCAMPHEYLBORANE Basic information |
| Product Name: | (+)-B-METHOXYDIISOPINOCAMPHEYLBORANE | | Synonyms: | (+)-B-METHOXYDIISOPINOCAMPHEYLBORANE;(+)-DIISOPINOCAMPHEYLMETHOXYBORANE;(-)-B-Methoxydiisopinocampheylborane;)-B-Methoxydiisopinocampheylborane;methoxy-bis[(1R,3S,4R,5R)-4,6,6-trimethyl-3-bicyclo[3.1.1]heptanyl]borane;Borinic acid, B,B-bis[(1R,2S,3R,5R)-2,6,6-trimethylbicyclo[3.1.1]hept-3-yl]-, methyl ester;()-B-Methoxydiisopinocampheylborane;(-)-B-Methoxydiisopinocampheylborane hydrate | | CAS: | 85134-98-1 | | MF: | C21H37BO | | MW: | 316.33 | | EINECS: | | Product Categories: | | Mol File: | 85134-98-1.mol |
| (+)-B-METHOXYDIISOPINOCAMPHEYLBORANE Chemical Properties |
| Boiling point | 365.6±9.0 °C(Predicted) | | density | 0.95±0.1 g/cm3(Predicted) | | Fp | >230 °F | | storage temp. | 2-8°C | | optical activity | [α]20/D 72±3°, c = 1% in diethyl ether |
| (+)-B-METHOXYDIISOPINOCAMPHEYLBORANE Usage And Synthesis |
| Uses | Reactant involved in organic synthesis reactions such as:- Double allylboration for synthesis of fragments of tetrafibricin
- Anticancer cytotoxic monorhizopodin synthesis
- Annulation of cyclic allylsilanes
- Asymmetric synthesis of β-amino-α-hydroxy acid taxol side chain analogs
| | General Description | B-Methoxydiisopinocampheylborane (Ipc2BOMe) is an organoborane compound, which is prepared from excess α-pinene, borane dimethylsulfide, and methanol via the formation of an intermediate diisocampheylborane. Ipc2BOMe is used as a versatile reagent for the construction of C-C bonds in asymmetric synthesis. |
| (+)-B-METHOXYDIISOPINOCAMPHEYLBORANE Preparation Products And Raw materials |
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